Active compound combinations having insecticidal/acaricidal properties

ABSTRACT

The present invention relates to novel active compound combinations comprising at least one known compound of the formula (I) 
                         
and at least one further active compound, which combinations are highly suitable for controlling animal and microbial pests such as unwanted insects and/or unwanted acarida and/or unwanted nematodes.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is the National Stage entry of InternationalApplication No. PCT/EP2018/077873, filed 12 Oct. 2018, which claimspriority to European Patent Application No. 17197094.0, filed 18 Oct.2017.

BACKGROUND Field

The present invention relates to active compound combinations comprisingfirstly at least one compound of formula (I) as shown below and secondlyand at least one active compound of group (II) selected from (a)Insecticide Groups (IRAC (Insecticide Resistance Action Committee) modeof action classification groups; also designated as “IRAC classificationgroups”) (5), (6), (9), (15), (23), (25) and (29), and (b) compounds offormula (IIa) or (IIb) or (IIc) or (IIc′) as shown below. Suchcombinations are highly suitable for controlling animal and microbialpests, such as unwanted insects, especially acarids (mites), nematodesand as plant strengthening agents.

Description of Related Art

The compound of formula (I) and methods for its production are knownfrom WO 2013/092350 and its insecticidal action has been described.

However, the acaricidal and/or insecticidal efficacy and/or the activityspectrum and/or the compatibility of the known compounds with plants,especially with respect to crop plants, is not always satisfactory.Therefore, novel active compound combinations with improved propertiesare in great demand.

SUMMARY

It has now been found that an active compound combination comprising atleast one compound of the formula (I)

and at least one active compound of group (II) which is selected from

(a) Insecticide Groups (IRAC classification groups) (5), (6), (9), (15),(23), (25) and (29), or

(b) compounds of formula (IIa) or (IIb) or (IIc) or (IIc′),

is highly suitable for the control of animal and microbial pests as wellas plant strengthening agent. Especially, such active compoundcombinations have very good insecticidal, acaricidal and nematicidalproperties.

DETAILED DESCRIPTION OF A PREFERRED EMBODIMENT

In formula (I), the crossed double bond indicates that E- or Z-isomersof the compound are possible, i.e. the 5-membered ring might be presentin two different orientations. According to the invention, the compoundof formula (I) can be present in form of its E-isomer or in form of itsZ-isomer or in form of a mixture of both E- and Z-isomers.

Such active compound combinations are very suitable for controllinganimal and microbial pests such as insects and/or arachnids, especiallyacarids, and/or nematodes and/or fungi, and indirectly improve planthealth. Further, such active compound combinations can be used forreducing overall damage of plants and plant parts as well as losses inharvested fruits or vegetables caused by such pests, e.g. insects, mitesand phytopathogens. Further, such active compound combinations aresuitable as plant strengthening agents.

Surprisingly, the insecticidal effect and/or arachnicidal/acaricidaleffect and/or nematicidal effect and/or antimicrobial effect and/or thefungicidal effect and/or the plant-strengthening effect and/or theyield-increasing effect of the active compound combinations according tothe invention is substantially higher than the sum of the effects of theindividual active ingredients. There is an unpredictable realsynergistic effect and not just a complementary/additive effect.

The active compound combinations according to the invention preferablycomprise the compound of formula (I) and the compound of group (II) insynergistically effective amounts. Group II consists of

(a) Insecticide Groups (IRAC (Insecticide Resistance Action Committee)mode of action classification groups; also designated as “IRACclassification groups”) (5), (6), (9), (15), (23), (25) and (29), and

(b) compounds of formula (IIa) or (IIb) or (IIc) or (IIc′) as shownbelow.

Therefore, the at least one active compound of group (II) is selectedfrom (a) or (b). These groups (a) and (b) are further defined asfollows:

(a) Insecticide Groups (IRAC classification groups):

(5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators, suchas, for example, spinosyns, e.g. spinetoram and spinosad, wherein saidmentioned compounds are preferred.

(6) Glutamate-gated chloride channel (GluCl) allosteric modulators, suchas, for example, avermectins/milbemycins, for example abamectin,emamectin benzoate, lepimectin and milbemectin, wherein said mentionedcompounds are preferred.

(9) Chordotonal organ TRPV channel modulators, such as, for examplepymetrozine or pyrifluquinazone, wherein said mentioned compounds arepreferred.

(15) Inhibitors of chitin biosynthesis, type 0, such as, for example,bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron,flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron,teflubenzuron and triflumuron, wherein said mentioned compounds arepreferred.

(23) Inhibitors of acetyl CoA carboxylase, such as, for example,tetronic and tetramic acid derivatives, e.g. spirodiclofen, spiromesifenand spirotetramat, wherein said mentioned compounds are preferred.

(25) Mitochondrial complex II electron transport inhibitors, such as,for example, beta-ketonitrile derivatives, e.g. cyenopyrafen andcyflumetofen and carboxanilides, such as, for example, pyflubumide,wherein said mentioned compounds are preferred.

(29) Chordotonal organ Modulators (with undefined target site) such as,for example, flonicamid, wherein said mentioned compounds are preferred.

(b) Compounds of formula (IIa) or (IIb) or (IIc) or (IIc′):

Compound of formula (IIa):

(IIa), known from WO 2006/089633 A1.

Compound of formula (IIb):

(IIb), known from WO 2008/067911 A1.

Compound of formula (IIc):

Compound of formula (IIc′):

The compound of formula (IIc′) shall be understood to be the free enolof the compound of formula (IIc).

All mixing partners of group II can, if their functional groups enablethis, optionally form salts with suitable bases or acids. All mixingpartners of group II can include tautomeric forms, where applicable.

The active compounds of group II which are specified herein by their“common name” are known and described inter alia in “The PesticideManual”, 16th edition, The British Crop Protection Council and the RoyalSoc. of Chemistry, 2012 and the literature cited therein or can besearched in the internet (e.g. http://www.alanwood.net/pesticides).Particularly, reference shall be made to said Manual or website in orderto further specify such a mixing partner of group II, e.g. to provideits chemical structure, IUPAC name or its pesticidal activity. Furtherinformation about such a mixing partner of group II will be provided aswell, in particular it's composition in case that the mixing partner ofgroup II is itself a mixture, e.g. a mixture of enantiomers.

For example, from the data sheet for compound (II-10) “Spinosad”(http://www.alanwood.net/pesticides/spinosad.html) it becomes evidentthat “Spinosad” is a mixture of 50-95%(2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dioneand 50-5%(2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dione(IUPAC), has the CAS Registration No. 168316-95-8(131929-60-7+131929-63-0) and possesses insecticidal activity.

If, e.g. within this description, the common name of an active compoundis used, this in each case encompasses all common derivatives, such asthe esters and salts, and isomers, especially optical isomers,especially the commercial form or forms. If an ester or salt is referredto by the common name, this also refers in each case to all other commonderivatives, such as other esters and salts, the free acids and neutralcompounds, and isomers, especially optical isomers, especially thecommercial form or forms. The chemical compound names mentioned refer toat least one of the compounds encompassed by the common name, frequentlya preferred compound.

Methods and Uses

The invention also relates to methods for controlling animal ormicrobial pests, in which active compound combinations according to theinvention are allowed to act on the animal or microbial pests and/ortheir habitat. Preferably, the animal pest is an insect or arachnid oracarid pest. Such control of the animal or microbial pests is preferablyconducted in agriculture and forestry, and in material protection.Preferably excluded herefrom are methods for the surgical or therapeutictreatment of the human or animal body and diagnostic methods carried outon the human or animal body.

The invention also relates to the use of active compound combinationsaccording to the invention as pesticidal combinations, in particularcrop protection agents. In the context of the present application, theterm “pesticide” in each case also always comprises the term “cropprotection agent”.

The active compound combinations according to the invention arepreferably suitable for controlling animal and microbial pests.

The active compound combinations according to the invention areparticularly preferably suitable for controlling animal pests,especially insect or arachnid or acarid pests.

The active compound combinations according to the invention areparticularly preferably suitable for controlling microbial pests.

The active compound combinations according to the invention areparticularly preferably suitable for controlling nematodes.

Preferably excluded from such uses are uses for the surgical ortherapeutic treatment of the human or animal body and diagnostic methodscarried out on the human or animal body.

The active compound combinations according to the invention areparticularly preferably used as plant-strengthening agents.

If appropriate, the active compound combinations according to theinvention can, at certain concentrations or application rates, also beused as herbicides, safeners, growth regulators or agents to improveplant properties, or as microbicides, for example as fungicides,antimycotics, bactericides, viricides (including agents against viroids)or as agents against MLO (Mycoplasma-like organisms) and RLO(Rickettsia-like organisms). If appropriate, they can also be employedas intermediates or precursors for the synthesis of other activecompound compositions.

The invention also relates to a process for preparing a crop protectionagent, characterized in that an active compound combination according tothe invention is mixed with extenders and/or surfactants.

The invention also relates to the use of an active compound combinationaccording to the invention for treating plants or parts thereof selectedfrom the group consisting of citrus, pome fruits, stone fruits, tropicalfruits, nuts, berries, vegetables, cotton, soybean, grape, tea, coffee,maize, rice and ornamentals.

The person skilled in the art is aware that the terms “a” or “an”, asused in the present application, may, depending on the situation, mean“one (1)” “one (1) or more” or “at least one (1)”. Generally, the termrefers to the meaning of “one (1) or more” or “at least one (1)”.However, in one embodiment, the term “a” refers exclusively to “one(1)”.

In the context of the present invention, “control of pests” means areduction in infestation by harmful pests, compared with the untreatedplant measured as pesticidal efficacy, preferably a reduction by 25-50%,compared with the untreated plant (100%), more preferably a reduction by40-79%, compared with the untreated plant (100%); even more preferably,the infection by pests is entirely suppressed (by 70-100%). The controlmay be curative, i.e. for treatment of already infected plants, orprotective, for protection of plants which have not yet been infected.

In the context of the present invention, “control of microbial pests”means a reduction in infestation by harmful microorganisms, comparedwith the untreated plant measured as fungicidal efficacy, preferably areduction by 25-50%, compared with the untreated plant (100%), morepreferably a reduction by 40-79%, compared with the untreated plant(100%); even more preferably, the infection by harmful microorganisms isentirely suppressed (by 70-100%). The control may be curative, i.e. fortreatment of already infected plants, or protective, for protection ofplants which have not yet been infected.

Mites are arthropods belonging to the subclass Acari (also known asAcarina) of the class Arachnida. Bananas and plantains belong to thegenera Musa in the family Musaceae.

Citrus is a common term and genus (Citrus) of flowering plants in therue family, Rutaceae. The term Citrus includes orange (C. sinensis),lemon (C. limon), grapefruit (C. paradisi), and lime (various, mostly C.aurantifolia, the key lime).

Pome is a common term for fruits produced by flowering plants in thesubtribe Malinae of the family Rosaceae and for plants producing thesefruits. A pome is an accessory fruit composed of one or more carpelssurrounded by accessory tissue. Examples of plants that produce fruitclassified as a pome are apple, loquat, pear, Pyracantha, and quince.

Vegetable as used herein refers to an edible plant or its part selectedfrom the list consisting of flower bud vegetable such as broccoli,cauliflower, globe artichokes and capers; leaf vegetable such as kale,spinach (Spinacia oleracea), arugula (Eruca sativa), and lettuce(Lactuca sativa); stem vegetable such as kohlrabi; stem shoot vegetablesuch as asparagus, bamboo shoots, potatoes (Solanum tuberosum L) andsweet potatoes (Ipomoea batatas); root vegetable such as carrots (Daucuscarota), parsnips (Pastinaca sativa), beets (Beta vulgaris), andradishes (Raphanus sativus); bulb vegetable such as onion, garlic andshallots of genus Allium; tomato (Solanum lycopersicum), cucumber(Cucumis sativus), zucchini, squash and pumpkin of genus speciesCucurbita pepo, pepper (of family Solanaceae), eggplant; beans(Phaseolus vulgaris). and pea (Pisum sativum).

Stone fruit are all species of the Prunus genus. Examples of plants thatproduce fruit classified as a stone fruit are e.g. peaches, nectarines,plums, apricots, and cherries. Subtropical and tropical fruit are fruitproduced by plants native to the geographical and climatic region of thesubtropics or tropics. Examples of plants that produce fruit classifiedas a subtropical or tropical fruit are e.g avocado, banana, cherimoya,date, dragon fruit, durian, fig, guava, jackfruit, kiwi, lychee, mango,mangosteen, passion fruit, papaya, pineapple, persimmon, pomegranate,rambutan and star fruit. Nuts are referring to any hard-walled, ediblekernel such as e.g. almonds, Brazil nuts, cashews, hazelnuts,macadamias, peanuts, pecans, pine nuts, pistachios and walnuts.

Berries are any small edible fruit usually juicy, round, brightlycoloured, sweet or sour, and do not have a stone or pit, although seedsmay be present as e.g. blackberry, blueberry, cranberry, currant,elderberry, gooseberry, grape, raspberry, strawberry.

Ornamentals are plants grown for decorative purposes in gardens andlandscape design, as houseplants, for cut flowers and specimen display,e.g. roses, chrysanthemums, tulips, etc.

An individual embodiment refers to an active compound combinationaccording to the invention, wherein the compound of group (II) isselected from the group consisting of (a) Insecticide Groups (5), (6),(9), (15), (23), (25) and (29).

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the compound of group (II) isselected from the group consisting of (b) compounds of formula (IIa) or(IIb) or (IIc) or (IIc′).

The compound of the formula (I) has a chiral sulphoxide group so that itforms two enantiomers having (+) or (−) specific rotation:

For the two enantiomers of the compound of formula (I) it is to beunderstood that the (+) enantiomer is the (R)-enantiomer and the(S)-enantiomer is the (−) enantiomer, i.e. the compound of formula (I-A)is also to be designated as (R)-enantiomer and the compound of formula(I-B) is also to be designated as (S)-enantiomer.

In the synthesis from achiral starting materials the two enantiomers areformed in equal amounts so that a racemate is present. The separation ofthe racemate into the individual enantiomers is known from theliterature (cf. WO 2013/092350).

Accordingly, the present invention provides active compound combinationscomprising the racemate or the (+) or (−) enantiomer of the compound offormula (I) and at least one active compound of group (II). Preferably,the optically active, stereoisomeric forms of the compound of formula(I) and its salts are used according to the invention, especiallypreferably its (+) enantiomer.

An individual embodiment refers to active compound combinationscomprising the racemate or the (+) or (−) enantiomer of the E-isomer ofthe compound of formula (I) and at least one active compound of group(II). Preferably, the optically active, stereoisomeric forms of thecompound of formula (I) and its salts are used according to theinvention, especially preferably its (+) enantiomer.

Another individual embodiment refers to active compound combinationscomprising the racemate or the (+) or (−) enantiomer of the Z-isomer ofthe compound of formula (I) and at least one active compound of group(II). Preferably, the optically active, stereoisomeric forms of thecompound of formula (I) and its salts are used according to theinvention, especially preferably its (+) enantiomer.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the compound of formula (I) ispresent in form of its racemate.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the E-isomer of the compound offormula (I) is present in form of its racemate.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the Z-isomer of the compound offormula (I) is present in form of its racemate.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the compound of formula (I) ispresent in form of its (+) enantiomer, or is present in form of amixture of its (+) enantiomer and its (−) enantiomer which is enrichedin the (+) enantiomer, preferably in a mixing ratio of at least 60:40and increasingly preferably of at least 70:30, 75:25, 80:20, 85:15 und90:10 (+):(−) enantiomer.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the E-isomer of the compound offormula (I) is present in form of its (+) enantiomer, or is present inform of a mixture of its (+) enantiomer and its (−) enantiomer which isenriched in the (+) enantiomer, preferably in a mixing ratio of at least60:40 and increasingly preferably of at least 70:30, 75:25, 80:20, 85:15und 90:10 (+):(−) enantiomer.

Another individual embodiment refers to an active compound combinationaccording to the invention, wherein the Z-isomer of the compound offormula (I) is present in form of its (+) enantiomer, or is present inform of a mixture of its (+) enantiomer and its (−) enantiomer which isenriched in the (+) enantiomer, preferably in a mixing ratio of at least60:40 and increasingly preferably of at least 70:30, 75:25, 80:20, 85:15und 90:10 (+):(−) enantiomer.

Reference is also made to an active compound combination, wherein thecompound of formula (I) is present in form of its (−) enantiomer, or ispresent in form of a mixture of its (−) enantiomer and its (+)enantiomer which is enriched in the (−) enantiomer, preferably in amixing ratio of at least 60:40 and increasingly preferably of at least70:30, 75:25, 80:20, 85:15 und 90:10 (−):(+) enantiomer.

Reference is also made to an active compound combination, wherein theE-isomer of the compound of formula (I) is present in form of its (−)enantiomer, or is present in form of a mixture of its (−) enantiomer andits (+) enantiomer which is enriched in the (−) enantiomer, preferablyin a mixing ratio of at least 60:40 and increasingly preferably of atleast 70:30, 75:25, 80:20, 85:15 und 90:10 (−):(+) enantiomer.

Reference is also made to an active compound combination, wherein theZ-isomer of the compound of formula (I) is present in form of its (−)enantiomer, or is present in form of a mixture of its (−) enantiomer andits (+) enantiomer which is enriched in the (−) enantiomer, preferablyin a mixing ratio of at least 60:40 and increasingly preferably of atleast 70:30, 75:25, 80:20, 85:15 und 90:10 (−):(+) enantiomer.

In the following, more preferred compounds of group (II) are described:

(a) More preferred mixing partners from the Insecticide Groups (IRACclassification groups) (5), (6), (9), (15), (23), (25) and (29) are:

(II-1) abamectin (IUPAC-name: extended von Bayer nomenclature: mixtureof ≥80%(10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-6′-[(S)-sec-butyl]-21,24-dihydroxy-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranosideand ≤20%(10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-21,24-dihydroxy-6′-isopropyl-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside;or bridged fused ring systems nomenclature: mixture of ≥80%(2aE,4E,8E)-(5′S,6S,6′R,7S,11R,13S,15S,17aR,20R,20aR,20bS)-6′-[(S)-sec-butyl]-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20,20b-dihydroxy-5′,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranosideand ≤20%(2aE,4E,8E)-(5′S,6S,6′R,7S,11R,13S,15S,17aR,20R,20aR,20bS)-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20,20b-dihydroxy-6′-isopropyl-5′,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside;CAS Reg. No. 71751-41-2);

(II-2) emamectin benzoate (IUPAC-name: extended von Baeyer nomenclature:mixture of ≥90%(10E,14E,16E)-(1R,4S,5′S.6S,6′R,8R,12S,13S,20R,21R,24S)-6′-[(S)-sec-butyl]-21,24-dihydroxy-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-α-L-lyxo-hexapyranosyl)-α-L-arabino-hexapyranosidebenzoate and ≤10%(10E,14E,16E)-(1R,4S,5′S,6S,6′R,8R,12S,13S,20R,21R,24S)-21,24-dihydroxy-6′-isopropyl-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(5′,6′-dihydro-2′H-pyran)-12-yl2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-α-L-lyxo-hexapyranosyl)-α-L-arabino-hexapyranosidebenzoate; or bridged fused ring systems nomenclature: mixture of ≥90%(2aE,4E,8E)-(5′S,6S,6′R,7S,11R,13S,15S,17aR,20R,20aR,20bS)-6′-[(S)-sec-butyl]-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20,20b-dihydroxy-5′,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-α-L-lyxo-hexapyranosyl)-α-L-arabino-hexapyranosidebenzoate and ≤10%(2aE,4E,8E)-(5′S,6S,6′R,7S,11R,13S,15S,17aR,20R,20aR,20bS)-5′,6,6′,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20,20b-dihydroxy-6′-isopropyl-5′,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl2,6-dideoxy-3-O-methyl-4-O-(2,4,6-trideoxy-3-O-methyl-4-methylamino-α-L-lyxo-hexapyranosyl)-α-L-arabino-hexapyranosidebenzoate; CAS Reg. No. 155569-91-8 (formerly 137512-74-4 and179607-18-2));

(II-3) lepimectin (IUPAC-name: extended von Baeyer nomenclature: mixtureof 80-100%(10E,14E,16E)-(1R,4S,5′S,6R,CR,8R,12R,13S,20R,21R,24S)-6′-ethyl-21,24-dihydroxy-5′,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(tetrahydropyran)-12-yl(Z)-2-methoxyimino-2-phenylacetate and 20-0%(10E,14E,16E)-(1R,4S,5′S,6R,6′R,8R,12R,13S,20R,21R,24S)-21,24-dihydroxy-5′,6′,11,13,22-pentamethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(tetrahydropyran)-12-yl(Z)-2-methoxyimino-2-phenylacetate; or bridged fused ring systemsnomenclature: mixture of 80-100%(2aE,4E,8E)-(5′S,6S,6′R,7R,11R,13R,15S,17aR,20R,20aR,20bS)-6′-ethyl-3′,4′,5′,6,6′,7,10,11,14,15,17a,20,20a,20b-tetradecahydro-20,20b-dihydroxy-5′,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl(Z)-2-methoxyimino-2-phenylacetate and 20-0%(2aE,4E,8E)-(5′S,6S,6′R,7R,11R,13R,15S,17aR,20R,20aR,20bS)-3′,4′,5′,6,6′,7,10,11,14,15,17a,20,20a,20b-tetradecahydro-20,20b-dihydroxy-5′,6,6′,8,19-pentamethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-7-yl(Z)-2-methoxyimino-2-phenylacetate; CAS Reg. No. 171249-05-1 (6′-ethyl)and 171249-10-8 (6′-methyl));

(II-4) milbemectin (IUPAC-name: extended von Baeyer nomenclature:mixture of 70%(10E,14E,16E)-(1R,4S,5′S,6R,6′R,8R,13R,20R,21R,24S)-6′-ethyl-21,24-dihydroxy-5′,11,13,22-tetramethyl-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(tetrahydropyran)-2-oneand 30%(10E,14E,16E)-(1R,4S,5′S,6R,6′R,8R,13R,20R,21R,24S)-21,24-dihydroxy-5′,6′,11,13,22-pentamethyl-(3,7,19-trioxatetracyclo[15.6.1.1^(4,8).0^(20,24)]pentacosa-10,14,16,22-tetraene)-6-spiro-2′-(tetrahydropyran)-2-one;or bridged fused ring systems nomenclature: mixture of 70%(2aE,4E,8E)-(5′S,6R,6′R,11R,13R,15S,17aR,20R,20aR,20bS)-6′-ethyl-3′,4′,5′,6,6′,7,10,11,14,15,17a,20,20a,20b-tetradecahydro-20,20b-dihydroxy-5′,6,8,19-tetramethylspiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-17-oneand 30%(2aE,4E,8E)-(5′S,6R,6′R,11R,13R,15S,17aR,20R,20aR,20bS)-3′,4′,5′,6,6′,7,10,11,14,15,17a,20,20a,20b-tetradecahydro-20,20b-dihydroxy-5′,6,6′,8,19-pentamethylspiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2′-[2H]pyran]-17-one;CAS Reg. No. 51596-10-2 (milbemycin A₃)+51596-11-3 (milbemycin A₄));

(II-5) spirodiclofen (IUPAC-name:3-(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl2,2-dimethylbutyrate; CAS Reg. No. 148477-71-8);

(II-6) spiromesifen (IUPAC-name:3-mesityl-2-oxo-1-oxaspiro[4.4]non-3-en-4-yl 3,3-dimethylbutyrate; CASReg. No. 283594-90-1);

(II-7) spirotetramat (IUPAC-name:cis-4-(ethoxycarbonyloxy)-8-methoxy-3-(2,5-xylyl)-1-azaspiro[4.5]dec-3-en-2-one;CAS Reg. No. 203313-25-1);

(II-8) cyenopyrafen (IUPAC-name:(E)-2-(4-tert-butylphenyl)-2-cyano-1-(1,3,4-trimethylpyrazol-5-yl)vinyl2,2-dimethylpropionate; CAS Reg. No. 560121-52-0);

(II-9) cyflumetofen (IUPAC-name: 2-methoxyethyl(RS)-2-(4-tert-butylphenyl)-2-cyano-3-oxo-3-(α,α,α-trifluoro-o-tolyl)propionate;CAS Reg. No. 400882-07-7);

(II-10) spinosad (IUPAC-name: mixture of 50-95%(2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dioneand 50-5%(2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-13-D-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dione;CAS Reg. No. 168316-95-8 (131929-60-7+131929-63-0));

(II-11) spinetoram (IUPAC-name: bridged fused ring systems nomenclature:mixture of 50-90%(2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyloxy)-13-[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methylpyran-2-yloxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecine-7,15-dioneand 50-10%(2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyloxy)-13-[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methylpyran-2-yloxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-4,14-dimethyl-1H-as-indaceno[3,2-c]oxacyclododecine-7,15-dione;or extended von Baeyer nomenclature: mixture of 50-90%(1S,2R,5R,7R,9R,10S,14R,15S,19S)-7-(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyloxy)-15-[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methylpyran-2-yloxy]-19-ethyl-14-methyl-20-oxatetracyclo[10.10.0.0^(2,10).0^(5,9)]docos-11-ene-13,21-dioneand 50-10%(1S,2S,5R,7S,9S,10S,14R,15S,19S)-7-(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyloxy)-15-[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methylpyran-2-yloxy]-19-ethyl-4,14-dimethyl-20-oxatetracyclo[10.10.0.0^(2,10).0^(5,9)]docosa-3,11-diene-13,21-dione;CAS Reg. No. 187166-40-1+187166-15-0);

(II-12) flonicamid (IUPAC-name:N-cyanomethyl-4-(trifluoromethyl)nicotinamide; CAS Reg. No.158062-67-0);

(II-13) pymetrozine (IUPAC-name:(E)-4,5-dihydro-6-methyl-4-(3-pyridylmethyleneamino)-1,2,4-triazin-3(2H)-one;CAS Reg. No. 123312-89-0);

(II-14) pyflubumide (IUPAC-name:3′-isobutyl-N-isobutyryl-1,3,5-trimethyl-4′-[2,2,2-trifluoro-1-methoxy-1-(trifluoromethyl)ethyl]pyrazole-4-carboxanilide;CAS Reg. No. 926914-55-8).

Especially preferred mixing partners from the Insecticide Groups (IRACclassification groups) (5), (6), (9), (15), (23), (25) and (29) are:

(II-1) abamectin, (II-2) emamectin benzoate, (II-4) milbemectin, (II-6)spiromesifen, (II-7) spirotetramat, (II-8) cyenopyrafen, (II-9)cyflumetofen, (II-10) spinosad and (II-14) pyflubumide.

One preferred embodiment refers to combinations comprising a compound offormula (I) and a compound of group (II) selected from the mixingpartners from the Insecticide Groups (IRAC classification groups) (5),(6), (9), (15), (23), (25) and (29) defined above as being preferred.

One preferred embodiment refers to combinations comprising a compound offormula (I) and a compound of group (II) selected from the mixingpartners from the Insecticide Groups (IRAC classification groups) (5),(6), (9), (15), (23), (25) and (29) defined above as being morepreferred.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and a compound of group (II) selected from themixing partners from the Insecticide Groups (IRAC classification groups)(5), (6), (9), (15), (23), (25) and (29) defined above as beingespecially preferred.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-1) abamectin.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-2) emamectin benzoate.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-4) milbemectin.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-6) spiromesifen.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-7) spirotetramat.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-8) cyenopyrafen.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-9) cyflumetofen.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-10) spinosad.

Another preferred embodiment refers to combinations comprising acompound of formula (I) and (II-14) pyflubumide.

(b) More preferred mixing partners from the group consisting of (b)compounds of formula (IIa) or (IIb) or (IIc) or (IIc′) are:

Compound of formula (IIa), compound of formula (IIb), compound offormula (IIc), compound of formula (IIc′).

Especially preferred mixing partners from the group consisting of (b)compounds of formula (IIa) or (IIb) are:

Compound of formula (IIa), compound of formula (IIb).

Another preferred embodiment refers to combinations comprising acompound of formula (I) and a compound of formula (IIa).

Another preferred embodiment refers to combinations comprising acompound of formula (I) and a compound of formula (IIb).

Another individual embodiment refers to combinations comprising acompound of formula (I) and a compound of formula (IIc).

Another individual embodiment refers to combinations comprising acompound of formula (I) and a compound of formula (IIc′).

Mixing Ratio

The synergistic effect is particularly pronounced when the activecompounds in the active compound combinations according to the inventionare present in certain weight ratios. However, the weight ratios of theactive compounds in the active compound combinations can be variedwithin a relatively wide range. In general, the combinations accordingto the invention comprise an active compound (I) and an active compoundof group (II) selected from (a) Insecticide Groups (5), (6), (9), (15),(23), (25) and (29) and (b) compounds of formula (IIa) or (IIb) or (IIc)or (IIc′) in the following preferred, more preferred and particularlypreferred mixing ratios:

Preferred mixing ratio: 125:1 to 1:125 such as 100:1 to 1:100 or 75:1 to1:75.

More preferred mixing ratio: 50:1 to 1:50 such as 50:1 to 1:15 or 1:15to 50:1 or even 20:1 to 1:20 or 20:1 to 1:15 or 15:1 to 1:20 or 15:1 to1:15 or 10:1 to 1:10 or 5:1 to 1:5.

Particularly preferred mixing ratios for some specific combinations ofcompound of formula (I) and a compound of group (II) are provided intable 1. Thus, each individual active compound combination of a compoundof formula (I) and the indicated mixing partner of group (II) in each ofthe indicated mixing ratios is a preferred embodiment of the invention.

TABLE 1 Mixing partner of group (II) Mixing ratios (II-1) abamectin400:1 to 1:1 or 400:1 to 20:1 or 20:1 to 2:1 (II-2) emamectin benzoate50:1 to 1:1 or 40:1 to 1:1 or 40:1 to 4:1 (II-4) milbemectin 25:1 to 1:5or 5:1 to 1:5 or 1:1 to 1:2.5 (II-6) spiromesifen 20:1 to 1:10 or 10:1to 1:5 or 10:1 to 1:1 (II-7) spirotetramat 30:1 to 1:30 or 10:1 to 1:30(II-8) cyenopyrafen 10:1 to 1:10 or 5:1 to 1:5 or 4:1 to 1:3 or 4:1(II-9) cyflumetofen 10:1 to 1:20 or 5:1 to 1:5 or 2:1 to 1:2 or 1:1(II-10) spinosad 10:1 to 1:10 or 5:1 to 1:5 or 4:1 to 1:1 or 4:1 (II-14)pyflubumide 20:1 to 1:20 or 10:1 to 1:10 or 10:1 to 1:1 compound offormula (IIa) 10:1 to 1:10 or 5:1 to 1:5 or 1:1 to 1:3 or 1:2 compoundof formula (IIb) 10:1 to 1:10 or 5:1 to 1:5 or 2:1 to 1:2 or 1:1compound of formula (IIc) 10:1 to 1:10 or 5:1 to 1:5 or 2:1 to 1:2 or1:1 compound of formula (IIc′) 10:1 to 1:10 or 5:1 to 1:5 or 2:1 to 1:2or 1:1

The mixing ratios are based on weight ratios. The ratio is to beunderstood as meaning active compound of the formula (I): an activecompound of group (II).

Additional Mixing Partners

Furthermore, the active compound combinations according to the inventionand, in particular, the active compound combinations listed in table 1,may contain one or more further active substances selected from afungicide, an insecticide or a biological control agent, i.e. at leastone further fungicidally or insecticidally active additive. Preferably,such further active additive is selected from groups (1) to (30)mentioned below. The active compounds identified here by their commonnames are known and are described, for example, in the pesticidehandbook (“The Pesticide Manual” 16th Ed., British Crop ProtectionCouncil 2012) or can be found on the Internet (e.g.http://www.alanwood.net/pesticides). The classification is based on thecurrent IRAC Mode of Action Classification Scheme at the time of filingof this patent application.

(1) Acetylcholinesterase (AChE) inhibitors, preferably carbamatesselected from alanycarb, aldicarb, bendiocarb, benfuracarb,butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan,ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb,methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur,thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb, ororganophosphates selected from acephate, azamethiphos, azinphos-ethyl,azinphos-methyl, cadusafos, chlorethoxyfos, chlorfenvinphos,chlormephos, chlorpyrifos-methyl, coumaphos, cyanophos,demeton-S-methyl, diazinon, dichlorvos/DDVP, dicrotophos, dimethoate,dimethylvinphos, disulfoton, EPN, ethion, ethoprophos, famphur,fenamiphos, fenitrothion, fenthion, fosthiazate, heptenophos, imicyafos,isofenphos, isopropyl O-(methoxyaminothiophosphoryl) salicylate,isoxathion, malathion, mecarbam, methamidophos, methidathion, mevinphos,monocrotophos, naled, omethoate, oxydemeton-methyl, parathion-methyl,phenthoate, phorate, phosalone, phosmet, phosphamidon, phoxim,pirimiphos-methyl, profenofos, propetamphos, prothiofos, pyraclofos,pyridaphenthion, quinalphos, sulfotep, tebupirimfos, temephos, terbufos,tetrachlorvinphos, thiometon, triazophos, triclorfon and vamidothion.

(2) GABA-gated chloride channel blockers, preferablycyclodiene-organochlorines selected from chlordane and endosulfan orphenylpyrazoles (fiproles), for example ethiprole and fipronil.

(3) Sodium channel modulators, preferably pyrethroids selected fromacrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin,bifenthrin, bioallethrin, bioallethrin s-cyclopentenyl isomer,bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin,lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin,beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin[(1R)-trans-isomer], deltamethrin, empenthrin [(EZ)-(1R)-isomer],esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate,flumethrin, tau-fluvalinate, halfenprox, imiprothrin, kadethrin,momfluorothrin, permethrin, phenothrin [(1R)-trans-isomer], prallethrin,pyrethrins (pyrethrum), resmethrin, silafluofen, tefluthrin,tetramethrin, tetramethrin [(1R)-isomer)], tralomethrin andtransfluthrin or DDT or methoxychlor.

(4) Nicotinic acetylcholine receptor (nAChR) competitive modulators,preferably neonicotinoids selected from acetamiprid, clothianidin,dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam ornicotine or sulfoxaflor or flupyradifurone.

(5) Nicotinic acetylcholine receptor (nAChR) allosteric modulators,preferably spinosyns selected from spinetoram and spinosad.

(6) Glutamate-gated chloride channel (GluCl) allosteric modulators,preferably avermectins/milbemycins selected from abamectin, emamectinbenzoate, lepimectin and milbemectin.

(7) Juvenile hormone mimics, preferably juvenile hormone analoguesselected from hydroprene, kinoprene and methoprene, or fenoxycarb orpyriproxyfen.

(8) Miscellaneous non-specific (multi-site) inhibitors, preferably alkylhalides selected from methyl bromide and other alkyl halides, orchloropicrine or sulphuryl fluoride or borax or tartar emetic or methylisocyanate generators selected from diazomet and metam.

(9) Chordotonal organ TRPV channel modulators selected from pymetrozineand pyrifluquinazone.

(10) Mite growth inhibitors selected from clofentezine, hexythiazox,diflovidazin and etoxazole.

(11) Microbial disruptors of the insect gut membrane selected fromBacillus thuringiensis subspecies israelensis, Bacillus sphaericus,Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensissubspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis, andB.t. plant proteins selected from Cry1Ab, Cry1Ac, Cry1Fa, Cry1A.105,Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb and Cry34Ab1/35Ab1.

(12) Inhibitors of mitochondrial ATP synthase, preferably ATP disruptorsselected from diafenthiuron, or organotin compounds selected fromazocyclotin, cyhexatin and fenbutatin oxide, or propargite ortetradifon.

(13) Uncouplers of oxidative phosphorylation via disruption of theproton gradient selected from chlorfenapyr, DNOC and sulfluramid.

(14) Nicotinic acetylcholine receptor channel blockers selected frombensultap, cartap hydrochloride, thiocylam and thiosultap-sodium.

(15) Inhibitors of chitin biosynthesis, type 0, selected frombistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron,flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron,teflubenzuron and triflumuron.

(16) Inhibitors of chitin biosynthesis, type 1 selected from buprofezin.

(17) Moulting disruptor (in particular for Diptera, i.e. dipterans)selected from cyromazine.

(18) Ecdysone receptor agonists selected from chromafenozide,halofenozide, methoxyfenozide and tebufenozide.

(19) Octopamine receptor agonists selected from amitraz.

(20) Mitochondrial complex III electron transport inhibitors selectedfrom hydramethylnone, acequinocyl and fluacrypyrim.

(21) Mitochondrial complex I electron transport inhibitors, preferablyMETI acaricides selected from fenazaquin, fenpyroximate, pyrimidifen,pyridaben, tebufenpyrad and tolfenpyrad, or rotenone (Derris).

(22) Voltage-dependent sodium channel blockers selected from indoxacarband metaflumizone.

(23) Inhibitors of acetyl CoA carboxylase, preferably tetronic andtetramic acid derivatives selected from spirodiclofen, spiromesifen andspirotetramat.

(24) Mitochondrial complex IV electron transport inhibitors, preferablyphosphines selected from aluminium phosphide, calcium phosphide,phosphine and zinc phosphide, or cyanides selected from calcium cyanide,potassium cyanide and sodium cyanide.

(25) Mitochondrial complex II electron transport inhibitors, preferablybeta-ketonitrile derivatives selected from cyenopyrafen andcyflumetofen, and carboxanilides selected from pyflubumide.

(28) Ryanodine receptor modulators, preferably diamides selected fromchlorantraniliprole, cyantraniliprole and flubendiamide.

(29) Chordotonal organ Modulators (with undefined target site) selectedfrom flonicamid.

(30) further active compounds selected from Afidopyropen, Afoxolaner,Azadirachtin, Benclothiaz, Benzoximate, Bifenazate, Broflanilide,Bromopropylate, Chinomethionat, Chloroprallethrin, Cryolite,Cyclaniliprole, Cycloxaprid, Cyhalodiamide, Dicloromezotiaz, Dicofol,epsilon-Metofluthrin, epsilon-Momfluthrin, Flometoquin,Fluazaindolizine, Fluensulfone, Flufenerim, Flufenoxystrobin,Flufiprole, Fluhexafon, Fluopyram, Fluralaner, Fluxametamide,Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione,kappa-Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin,Paichongding, Pyridalyl, Pyrifluquinazon, Pyriminostrobin,Spirobudiclofen, Tetramethylfluthrin, Tetraniliprole,Tetrachlorantraniliprole, Tigolaner, Tioxazafen, Thiofluoximate,Triflumezopyrim and iodomethane; furthermore preparations based onBacillus finnus (I-1582, BioNeem, Votivo), and also the followingcompounds:1-{2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulphinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine(known from WO2006/043635) (CAS 885026-50-6),{1′-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]-5-fluorospiro[indol-3,4′-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methanone(known from WO2003/106457) (CAS 637360-23-7),2-chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)prop-2-en-1-yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide(known from WO2006/003494) (CAS 872999-66-1),3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diazaspiro[4.5]dec-3-en-2-one(known from WO 2010052161) (CAS 1225292-17-0),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-ylethyl carbonate (known from EP2647626) (CAS 1440516-42-6),4-(but-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoropyrimidine(known from WO2004/099160) (CAS 792914-58-0), PF1364 (known fromJP2010/018586) (CAS 1204776-60-2),N-[(2E)-1-[(6-chloropyridin-3-yl)methyl]pyridin-2(1H)-ylidene]-2,2,2-trifluoroacetamide(known from WO2012/029672) (CAS 1363400-41-2),(3E)-3-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoro-propan-2-one(known from WO2013/144213) (CAS 1461743-15-6),N-[3-(benzylcarbamoyl)-4-chlorophenyl]-1-methyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxamide(known from WO2010/051926) (CAS 1226889-14-0),5-bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide(known from CN103232431) (CAS 1449220-44-3),4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)-benzamide,4-[5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-soxazolyl]-2-methyl-N-(trans-1-oxido-3-thietanyl)-benzamideand4-[(5S)-5-(3,5-dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1-oxido-3-thietanyl)benzamide(known from WO 2013/050317 A1) (CAS 1332628-83-7),N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide,(+)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamideand(−)-N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)sulfinyl]-propanamide(known from WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 A1)(CAS 1477923-37-7),5-[[(2E)-3-chloro-2-propen-1-yl]amino]-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile(known from CN 101337937 A) (CAS 1105672-77-2),3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)thioxomethyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide,(Liudaibenjiaxuanan, known from CN 103109816 A) (CAS 1232543-85-9);N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-Pyrazole-5-carboxamide(known from WO 2012/034403 A1) (CAS 1268277-22-0),N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(known from WO 2011/085575 A1) (CAS 1233882-22-8),4-[3-[2,6-dichloro-4-[(3,3-dichloro-2-propen-1-yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluoromethyl)-pyrimidine(known from CN 101337940 A) (CAS 1108184-52-6); (2E)- and2(Z)-2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide(known from CN 101715774 A) (CAS 1232543-85-9);3-(2,2-dichloroethenyl)-2,2-dimethyl-4-(1H-benzimidazol-2-yl)phenyl-cyclopropanecarboxylicacid ester (known from CN 103524422 A) (CAS 1542271-46-4);(4aS)-7-chloro-2,5-dihydro-2-[[(methoxycarbonyl)[4-[(trifluoromethyl)thio]phenyl]amino]carbonyl]-indeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylic acidmethyl ester (known from CN 102391261 A) (CAS 1370358-69-2);6-deoxy-3-O-ethyl-2,4-di-O-methyl-,1-[N-[4-[1-[4-(1,1,2,2,2-pentafluoroethoxy)phenyl]-1H-1,2,4-triazol-3-yl]phenyl]carbamate]-α-L-mannopyranose(known from US 2014/0275503 A1) (CAS 1181213-14-8);8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(CAS 1253850-56-4),(8-anti)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(CAS 933798-27-7),(8-syn)-8-(2-cyclopropylmethoxy-4-trifluoromethyl-phenoxy)-3-(6-trifluoromethyl-pyridazin-3-yl)-3-aza-bicyclo[3.2.1]octane(known from WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8),N-[3-chloro-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluoropropyl)thio]-propanamide(known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) andN-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(known from CN 103265527 A) (CAS 1452877-50-7),5-(1,3-dioxan-2-yl)-4-[[4-(trifluoromethyl)phenyl] methoxy]-pyrimidine(known from WO 2013/115391 A1) (CAS 1449021-97-9),3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1-methyl-1,8-diazaspiro[4.5]dec-3-en-2-one(known from WO 2010/066780 A1, WO 2011/151146 A1) (CAS 1229023-34-0),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione(known from WO 2014/187846 A1) (CAS 1638765-58-8),3-(4-chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carbonicacid ethyl ester (known from WO 2010/066780 A1, WO 2011151146 A1) (CAS1229023-00-0),N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide(known from DE 3639877 A1, WO 2012029672 A1) (CAS 1363400-41-2),[N(E)]-N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,(known from WO 2016005276 A1) (CAS 1689566-03-7),[N(Z)]-N-[1-[(6-chloro-3-pyridinyl)methyl]-2(1H)-pyridinylidene]-2,2,2-trifluoro-acetamide,(CAS 1702305-40-5),3-endo-3-[2-propoxy-4-(trifluoromethyl)phenoxy]-9-[[5-(trifluoromethyl)-2-pyridinyl]oxy]-9-azabicyclo[3.3.1]nonane(known from WO 2011/105506 A1, WO 2016/133011 A1) (CAS 1332838-17-1).

The active compound combinations can preferably be used as pesticides.They are active against normally sensitive and resistant species andagainst all or some stages of development. The abovementioned pestsinclude:

pests from the phylum of the Arthropoda, in particular from the class ofthe Arachnida, for example Acarus spp., for example Acarus siro, Aceriakuko, Aceria sheldoni, Aculops spp., Aculus spp., for example Aculusfockeui, Aculus schlechtendali, Amblyomma spp., Amphitetranychusviennensis, Argas spp., Boophilus spp., Brevipalpus spp., for exampleBrevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroidesspp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoidespteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychusspp., for example Eotetranychus hicoriae, Epitrimerus pyri,Eutetranychus spp., for example Eutetranychus banksi, Eriophyes spp.,for example Eriophyes pyri, Glycyphagus domesticus, Halotydeusdestructor, Hemitarsonemus spp., for example Hemitarsonemus latus(=Polyphagotarsonemus latus), Hyalomma spp., Ixodes spp., Latrodectusspp., Loxosceles spp., Neutrombicula autumnalis, Nuphersa spp.,Oligonychus spp., for example Oligonychus coffeae, Oligonychusconiferarum, Oligonychus ilicis, Oligonychus indicus, Oligonychusmangiferus, Oligonychus pratensis, Oligonychus punicae, Oligonychusyothersi, Ornithodorus spp., Ornithonyssus spp., Panonychus spp., forexample Panonychus citri (=Metatetranychus citri), Panonychus ulmi(=Metatetranychus ulmi), Phyllocoptruta oleivora, Platytetranychusmultidigituli, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalusspp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus,Steneotarsonemus spp., Steneotarsonemus spinki, Tarsonemus spp., forexample Tarsonemus confusus, Tarsonemus pallidus, Tetranychus spp., forexample Tetranychus canadensis, Tetranychus cinnabarinus, Tetranychusturkestani, Tetranychus urticae, Trombicula alfreddugesi, Vaejovis spp.,Vasates lycopersici;

from the class of the Chilopoda, for example Geophilus spp., Scutigeraspp.;

from the order or the class of the Collembola, for example Onychiurusarmatus; Sminthurus viridis;

from the class of the Diplopoda, for example Blaniulus guttulatus;

from the class of the Insecta, for example from the order of theBlattodea, for example Blatta orientalis, Blattella asahinai, Blattellagermanica, Leucophaea maderae, Loboptera decipiens, Neostylopygarhombifolia, Panchlora spp., Parcoblatta spp., Periplaneta spp., forexample Periplaneta americana, Periplaneta australasiae, Pycnoscelussurinamensis, Supella longipalpa;

from the order of the Coleoptera, for example Acalymma vittatum,Acanthoscelides obtectus, Adoretus spp., Aethina tumida, Agelasticaalni, Agrilus spp., for example Agrilus planipennis, Agrilus coxalis,Agrilus bilineatus, Agrilus anxius, Agriotes spp., for example Agrioteslinneatus, Agriotes mancus, Alphitobius diaperinus, Amphimallonsolstitialis, Anobium punctatum, Anoplophora spp., for exampleAnoplophora glabripennis, Anthonomus spp., for example Anthonomusgrandis, Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., forexample Atomaria linearis, Attagenus spp., Baris caerulescens,Bruchidius obtectus, Bruchus spp., for example Bruchus pisorum, Bruchusrufimanus, Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., forexample Ceutorrhynchus assimilis, Ceutorrhynchus quadridens,Ceutorrhynchus rapae, Chaetocnema spp., for example Chaetocnemaconfinis, Chaetocnema denticulata, Chaetocnema ectypa, Cleonus mendicus,Conoderus spp., Cosmopolites spp., for example Cosmopolites sordidus,Costelytra zealandica, Ctenicera spp., Curculio spp., for exampleCurculio caryae, Curculio caryatrypes, Curculio obtusus, Curculio sayi,Cryptolestes ferrugineus, Cryptolestes pusillus, Cryptorhynchus lapathi,Cryptorhynchus mangiferae, Cylindrocopturus spp., Cylindrocopturusadspersus, Cylindrocopturus furnissi, Dendroctonus spp., for exampleDendroctonus ponderosae, Dermestes spp., Diabrotica spp., for exampleDiabrotica balteata, Diabrotica barberi, Diabrotica undecimpunctatahowardi, Diabrotica undecimpunctata undecimpunctata, Diabroticavirgifera virgifera, Diabrotica virgifera zeae, Dichocrocis spp.,Dicladispa armigera, Diloboderus spp., Epicaerus spp., Epilachna spp.,for example Epilachna borealis, Epilachna varivestis, Epitrix spp., forexample Epitrix cucumeris, Epitrix fuscula, Epitrix hirtipennis, Epitrixsubcrinita, Epitrix tuberis, Faustinus spp., Gibbium psylloides,Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Heteronyxspp., Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypomecessquamosus, Hypothenemus spp., for example Hypothenemus hampei,Hypothenemus obscurus, Hypothenemus pubescens, Lachnosternaconsanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp.,Lema spp., Leptinotarsa decemlineata, Leucoptera spp., for exampleLeucoptera coffeella, Limonius ectypus, Lissorhoptrus oryzophilus,Listronotus (=Hyperodes) spp., Lixus spp., Luperodes spp., Luperomorphaxanthodera, Lyctus spp., Megacyllene spp., for example Megacyllenerobiniae, Megascelis spp., Melanotus spp., for example Melanotuslongulus oregonensis, Meligethes aeneus, Melolontha spp., for exampleMelolontha melolontha, Migdolus spp., Monochamus spp., Naupactusxanthographus, Necrobia spp., Neogalerucella spp., Niptus hololeucus,Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae,Otiorhynchus spp., for example Otiorhynchus cribricollis, Otiorhynchusligustici, Otiorhynchus ovatus, Otiorhynchus rugosostriarus,Otiorhynchus sulcatus, Oulema spp., for example Oulema melanopus, Oulemaoryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp.,Phyllophaga helleri, Phyllotreta spp., for example Phyllotretaarmoraciae, Phyllotreta pusilla, Phyllotreta ramosa, Phyllotretastriolata, Popillia japonica, Premnotrypes spp., Prostephanus truncatus,Psylliodes spp., for example Psylliodes affinis, Psylliodeschrysocephala, Psylliodes punctulata, Ptinus spp., Rhizobius ventralis,Rhizopertha dominica, Rhynchophorus spp., Rhynchophorus ferrugineus,Rhynchophorus palmarum, Scolytus spp., for example Scolytusmultistriatus, Sinoxylon perforans, Sitophilus spp., for exampleSitophilus granarius, Sitophilus linearis, Sitophilus oryzae, Sitophiluszeamais, Sphenophorus spp., Stegobium paniceum, Sternechus spp., forexample Sternechus paludatus, Symphyletes spp., Tanymecus spp., forexample Tanymecus dilaticollis, Tanymecus indicus, Tanymecus palliatus,Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., for exampleTribolium audax, Tribolium castaneum, Tribolium confusum, Trogodermaspp., Tychius spp., Xylotrechus spp., Zabrus spp., for example Zabrustenebrioides;

from the order of the Dermaptera, for example Anisolabis maritime,Forficula auricularia, Labidura riparia;

from the order of the Diptera, for example Aedes spp., for example Aedesaegypti, Aedes albopictus, Aedes sticticus, Aedes vexans, Agromyza spp.,for example Agromyza frontella, Agromyza parvicornis, Anastrepha spp.,Anopheles spp., for example Anopheles quadrimaculatus, Anophelesgambiae, Asphondylia spp., Bactrocera spp., for example Bactroceracucurbitae, Bactrocera dorsalis, Bactrocera oleae, Bibio hortulanus,Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata,Chironomus spp., Chrysomya spp., Chrysops spp., Chrysozona pluvialis,Cochliomya spp., Contarinia spp., for example Contarinia johnsoni,Contarinia nasturtii, Contarinia pyrivora, Contarinia schulzi,Contarinia sorghicola, Contarinia tritici, Cordylobia anthropophaga,Cricotopus sylvestris, Culex spp., for example Culex pipiens, Culexquinquefasciatus, Culicoides spp., Culiseta spp., Cuterebra spp., Dacusoleae, Dasineura spp., for example Dasineura brassicae, Delia spp., forexample Delia antiqua, Delia coarctata, Delia florilega, Delia platura,Delia radicum, Dermatobia hominis, Drosophila spp., for exampleDrosphila melanogaster, Drosophila suzukii, Echinocnemus spp., Euleiaheraclei, Fannia spp., Gasterophilus spp., Glossina spp., Haematopotaspp., Hydrellia spp., Hydrellia griseola, Hylemya spp., Hippobosca spp.,Hypoderma spp., Liriomyza spp., for example Liriomyza brassicae,Liriomyza huidobrensis, Liriomyza sativae, Lucilia spp., for exampleLucilia cuprina, Lutzomyia spp., Mansonia spp., Musca spp., for exampleMusca domestica, Musca domestica vicina, Oestrus spp., Oscinella frit,Paratanytarsus spp., Paralauterborniella subcincta, Pegomya or Pegomyiaspp., for example Pegomya betae, Pegomya hyoscyami, Pegomya rubivora,Phlebotomus spp., Phorbia spp., Phormia spp., Piophila casei, Platypareapoeciloptera, Prodiplosis spp., Psila rosae, Rhagoletis spp., forexample Rhagoletis cingulata, Rhagoletis completa, Rhagoletis fausta,Rhagoletis indifferens, Rhagoletis mendax, Rhagoletis pomonella,Sarcophaga spp., Simulium spp., for example Simulium meridionale,Stomoxys spp., Tabanus spp., Tetanops spp., Tipula spp., for exampleTipula paludosa, Tipula simplex, Toxotrypana curvicauda;

from the order of the Hemiptera, for example Acizzia acaciaebaileyanae,Acizzia dodonaeae, Acizzia uncatoides, Acrida turrita, Acyrthosiponspp., for example Acyrthosiphon pisum, Acrogonia spp., Aeneolamia spp.,Agonoscena spp., Aleurocanthus spp., Aleyrodes proletella, Aleurolobusbarodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrascaspp., for example Amrasca bigutulla, Amrasca devastans, Anuraphiscardui, Aonidiella spp., for example Aonidiella aurantii, Aonidiellacitrina, Aonidiella inornata, Aphanostigma pini, Aphis spp., for exampleAphis citricola, Aphis craccivora, Aphis fabae, Aphis forbesi, Aphisglycines, Aphis gossypii, Aphis hederae, Aphis illinoisensis, Aphismiddletoni, Aphis nasturtii, Aphis nerii, Aphis pomi, Aphis spiraecola,Aphis viburniphila, Arboridia apicalis, Arytainilla spp., Aspidiellaspp., Aspidiotus spp., for example Aspidiotus nerii, Atanus spp.,Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis,Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp.,Brevicoryne brassicae, Cacopsylla spp., for example Cacopsylla pyricola,Calligypona marginata, Capulinia spp., Carneocephala fulgida,Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphonfragaefolii, Chionaspis tegalensis, Chlorita onukii, Chondracris rosea,Chromaphis juglandicola, Chrysomphalus aonidum, Chrysomphalus ficus,Cicadulina mbila, Coccomytilus halli, Coccus spp., for example Coccushesperidum, Coccus longulus, Coccus pseudomagnoliarum, Coccus viridis,Cryptomyzus ribis, Cryptoneossa spp., Ctenarytaina spp., Dalbulus spp.,Dialeurodes chittendeni, Dialeurodes citri, Diaphorina citri, Diaspisspp., Diuraphis spp., Doralis spp., Drosicha spp., Dysaphis spp., forexample Dysaphis apiifolia, Dysaphis plantaginea, Dysaphis tulipae,Dysmicoccus spp., Empoasca spp., for example Empoasca abrupta, Empoascafabae, Empoasca maligna, Empoasca solana, Empoasca stevensi, Eriosomaspp., for example Eriosoma americanum, Eriosoma lanigerum, Eriosomapyricola, Erythroneura spp., Eucalyptolyma spp., Euphyllura spp.,Euscelis bilobatus, Ferrisia spp., Fiorinia spp., Furcaspis oceanica,Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsyllaspinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopteruspruni, Icerya spp., for example Icerya purchasi, Idiocerus spp.,Idioscopus spp., Laodelphax striatellus, Lecanium spp., for exampleLecanium corni (=Parthenolecanium corni), Lepidosaphes spp., for exampleLepidosaphes ulmi, Lipaphis erysimi, Lopholeucaspis japonica, Lycormadelicatula, Macrosiphum spp., for example Macrosiphum euphorbiae,Macrosiphum lilii, Macrosiphum rosae, Macrosteles facifrons, Mahanarvaspp., Melanaphis sacchari, Metcalfiella spp., Metcalfa pruinosa,Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzusspp., for example Myzus ascalonicus, Myzus cerasi, Myzus ligustri, Myzusornatus, Myzus persicae, Myzus nicotianae, Nasonovia ribisnigri,Neomaskellia spp., Nephotettix spp., for example Nephotettix cincticepsNephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens,Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp.,Parabemisia myricae, Paratrioza spp., for example Paratrioza cockerelli,Parlatoria spp., Pemphigus spp., for example Pemphigus bursarius,Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccusspp., for example Phenacoccus madeirensis, Phloeomyzus passerinii,Phorodon humuli, Phylloxera spp., for example Phylloxera devastatrix,Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., forexample Planococcus citri, Prosopidopsylla flava, Protopulvinariapyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., for examplePseudococcus calceolariae, Pseudococcus comstocki, Pseudococcuslongispinus, Pseudococcus maritimus, Pseudococcus viburni, Psyllopsisspp., Psylla spp., for example Psylla buxi, Psylla mali, Psylla pyri,Pteromalus spp., Pulvinaria spp., Pyrilla spp., Quadraspidiotus spp.,for example Quadraspidiotus juglansregiae, Quadraspidiotusostreaeformis, Quadraspidiotus perniciosus, Quesada gigas, Rastrococcusspp., Rhopalosiphum spp., for example Rhopalosiphum maidis,Rhopalosiphum oxyacanthae, Rhopalosiphum padi, Rhopalosiphumrufiabdominale, Saissetia spp., for example Saissetia coffeae, Saissetiamiranda, Saissetia neglecta, Saissetia oleae, Scaphoideus titanus,Schizaphis graminum, Selenaspidus articulatus, Sipha flava, Sitobionavenae, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephalafestina, Siphoninus phillyreae, Tenalaphara malayensis, Tetragonocephelaspp., Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., forexample Toxoptera aurantii, Toxoptera citricidus, Trialeurodesvaporariorum, Trioza spp., for example Trioza diospyri, Typhlocyba spp.,Unaspis spp., Viteus vitifolii, Zygina spp.; from the suborder of theHeteroptera, for example Aelia spp., Anasa tristis, Antestiopsis spp.,Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Caveleriusspp., Cimex spp., for example Cimex adjunctus, Cimex hemipterus, Cimexlectularius, Cimex pilosellus, Collaria spp., Creontiades dilutus,Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercusspp., Euschistus spp., for example Euschistus heros, Euschistus servus,Euschistus tristigmus, Euschistus variolarius, Eurydema spp., Eurygasterspp., Halyomorpha halys, Heliopeltis spp., Horcias nobilellus,Leptocorisa spp., Leptocorisa varicornis, Leptoglossus occidentalis,Leptoglossus phyllopus, Lygocoris spp., for example Lygocoris pabulinus,Lygus spp., for example Lygus elisus, Lygus hesperus, Lygus lineolaris,Macropes excavatus, Megacopta cribraria, Miridae, Monalonion atratum,Nezara spp., for example Nezara viridula, Nysius spp., Oebalus spp.,Pentomidae, Piesma quadrata, Piezodorus spp., for example Piezodorusguildinii, Psallus spp., Pseudacysta persea, Rhodnius spp., Sahlbergellasingularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi,Tibraca spp., Triatoma spp.;

from the order of the Hymenoptera, for example Acromyrmex spp., Athaliaspp., for example Athalia rosae, Atta spp., Camponotus spp.,Dolichovespula spp., Diprion spp., for example Diprion similis,Hoplocampa spp., for example Hoplocampa cookei, Hoplocampa testudinea,Lasius spp., Linepithema (Iridiomyrmex) humile, Monomorium pharaonis,Paratrechina spp., Paravespula spp., Plagiolepis spp., Sirex spp., forexample Sirex noctilio, Solenopsis invicta, Tapinoma spp., Technomyrmexalbipes, Urocerus spp., Vespa spp., for example Vespa crabro, Wasmanniaauropunctata, Xeris spp.;

from the order of the Isopoda, for example Armadillidium vulgare,Oniscus asellus, Porcellio scaber;

from the order of the Isoptera, for example Coptotermes spp., forexample Coptotermes formosanus, Cornitermes cumulans, Cryptotermes spp.,Incisitermes spp., Kalotermes spp., Microtermes obesi, Nasutitermesspp., Odontotermes spp., Porotermes spp., Reticulitermes spp., forexample Reticulitermes flavipes, Reticulitermes hesperus;

from the order of the Lepidoptera, for example Achroia grisella,Acronicta major, Adoxophyes spp., for example Adoxophyes orana, Aedialeucomelas, Agrotis spp., for example Agrotis segetum, Agrotis ipsilon,Alabama spp., for example Alabama argillacea, Amyelois transitella,Anarsia spp., Anticarsia spp., for example Anticarsia gemmatalis,Argyroploce spp., Autographa spp., Barathra brassicae, Blastodacna atra,Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseolaspp., Cacoecia spp., Caloptilia theivora, Capua reticulana, Carpocapsapomonella, Carposina niponensis, Cheimatobia brumata, Chilo spp., forexample Chilo plejadellus, Chilo suppressalis, Choreutis pariana,Choristoneura spp., Chrysodeixis chalcites, Clysia ambiguella,Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp.,Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Cydia spp., forexample Cydia nigricana, Cydia pomonella, Dalaca noctuides, Diaphaniaspp., Diparopsis spp., Diatraea saccharalis, Dioryctria spp., forexample Dioryctria zimmermani, Earias spp., Ecdytolopha aurantium,Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., for exampleEphestia elutella, Ephestia kuehniella, Epinotia spp., Epiphyaspostvittana, Erannis spp., Erschoviella musculana, Etiella spp.,Eudocima spp., Eulia spp., Eupoecilia ambiguella, Euproctis spp., forexample Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleriamellonella, Gracillaria spp., Grapholitha spp., for example Grapholitamolesta, Grapholita prunivora, Hedylepta spp., Helicoverpa spp., forexample Helicoverpa armigera, Helicoverpa zea, Heliothis spp., forexample Heliothis virescens, Hofmannophila pseudospretella, Homoeosomaspp., Homona spp., Hyponomeuta padella, Kakivoria flavofasciata,Lampides spp., Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis,Leucoptera spp., for example Leucoptera coffeella, Lithocolletis spp.,for example Lithocolletis blancardella, Lithophane antennata, Lobesiaspp.,

for example Lobesia botrana, Loxagrotis albicosta, Lymantria spp., forexample Lymantria dispar, Lyonetia spp., for example Lyonetia clerkella,Malacosoma neustria, Maruca testulalis, Mamestra brassicae, Melanitisleda, Mocis spp., Monopis obviella, Mythimna separata, Nemapogoncloacellus, Nymphula spp., Oiketicus spp., Omphisa spp., Operophteraspp., Oria spp., Orthaga spp., Ostrinia spp., for example Ostrinianubilalis, Panolis flammea, Parnara spp., Pectinophora spp., for examplePectinophora gossypiella, Perileucoptera spp., Phthorimaea spp., forexample Phthorimaea operculella, Phyllocnistis citrella, Phyllonorycterspp., for example Phyllonorycter blancardella, Phyllonoryctercrataegella, Pieris spp., for example Pieris rapae, Platynota stultana,Plodia interpunctella, Plusia spp., Plutella xylostella (=Plutellamaculipennis), Podesia spp., for example Podesia syringae, Prays spp.,Prodenia spp., Protoparce spp., Pseudaletia spp., for examplePseudaletia unipuncta, Pseudoplusia includens, Pyrausta nubilalis,Rachiplusia nu, Schoenobius spp., for example Schoenobius bipunctifer,Scirpophaga spp., for example Scirpophaga innotata, Scotia segetum,Sesamia spp., for example Sesamia inferens, Sparganothis spp.,Spodoptera spp., for example Spodoptera eradiana, Spodoptera exigua,Spodoptera frugiperda, Spodoptera praefica, Stathmopoda spp., Stenomaspp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora,Thaumetopoea spp., Thermesia gemmatalis, Tinea cloacella, Tineapellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzella,Trichoplusia spp., for example Trichoplusia ni, Tryporyza incertulas,Tuta absoluta, Virachola spp.;

from the order of the Orthoptera or Saltatoria, for example Achetadomesticus, Dichroplus spp., Gryllotalpa spp., for example Gryllotalpagryllotalpa, Hieroglyphus spp., Locusta spp., for example Locustamigratoria, Melanoplus spp., for example Melanoplus devastator,Paratlanticus ussuriensis, Schistocerca gregaria;

from the order of the Phthiraptera, for example Damalinia spp.,Haematopinus spp., Linognathus spp., Pediculus spp., Phylloxeravastatrix, Phthirus pubis, Trichodectes spp.;

from the order of the Psocoptera, for example Lepinotus spp., Liposcelisspp.;

from the order of the Siphonaptera, for example, Ceratophyllus spp.,Ctenocephalides spp., for example Ctenocephalides canis, Ctenocephalidesfelis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis;

from the order of the Thysanoptera, for example Anaphothrips obscurus,Baliothrips biformis, Chaetanaphothrips leeuweni, Drepanothrips reuteri,Enneothrips flavens, Frankliniella spp., for example Frankliniellafusca, Frankliniella occidentalis, Frankliniella schultzei,Frankliniella tritici, Frankliniella vaccinii, Frankliniella williamsi,Haplothrips spp., Heliothrips spp., Hercinothrips femoralis, Kakothripsspp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothripscardamomi, Thrips spp., for example Thrips palmi, Thrips tabaci;

from the order of the Zygentoma (=Thysanura), for example Ctenolepismaspp., Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica;

from the class of the Symphyla, for example Scutigerella spp., forexample Scutigerella immaculata;

pests from the phylum of the Mollusca, for example from the class of theBivalvia, for example Dreissena spp.,

and also from the class of the Gastropoda, for example Anion spp., forexample Anion ater rufus, Biomphalaria spp., Bulinus spp., Derocerasspp., for example Deroceras laeve, Galba spp., Lymnaea spp., Oncomelaniaspp., Pomacea spp., Succinea spp.;

plant pests from the phylum of the Nematoda, i.e. phytoparasiticnematodes, in particular Aglenchus spp., for example Aglenchus agricola,Anguina spp., for example Anguina tritici, Aphelenchoides spp., forexample Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimusspp., for example Belonolaimus gracilis, Belonolaimus longicaudatus,Belonolaimus nortoni, Bursaphelenchus spp., for example Bursaphelenchuscocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus,Cacopaurus spp., for example Cacopaurus pestis, Criconemella spp., forexample Criconemella curvata, Criconemella onoensis, Criconemellaornata, Criconemella rusium, Criconemella xenoplax (=Mesocriconemaxenoplax), Criconemoides spp., for example Criconemoides ferniae,Criconemoides onoense, Criconemoides ornatum, Ditylenchus spp., forexample Ditylenchus dipsaci, Dolichodorus spp., Globodera spp., forexample Globodera pallida, Globodera rostochiensis, Helicotylenchusspp., for example Helicotylenchus dihystera, Hemicriconemoides spp.,Hemicycliophora spp., Heterodera spp., for example Heterodera avenae,Heterodera glycines, Heterodera schachtii, Hirschmaniella spp.,Hoplolaimus spp., Longidorus spp., for example Longidorus africanus,Meloidogyne spp., for example Meloidogyne chitwoodi, Meloidogyne fallax,Meloidogyne hapla, Meloidogyne incognita, Meloinema spp., Nacobbus spp.,Neotylenchus spp., Paralongidorus spp., Paraphelenchus spp.,Paratrichodorus spp., for example Paratrichodorus minor, Paratylenchusspp., Pratylenchus spp., for example Pratylenchus penetrans,Pseudohalenchus spp., Psilenchus spp., Punctodera spp., Quinisulciusspp., Radopholus spp., for example Radopholus citrophilus, Radopholussimilis, Rotylenchulus spp., Rotylenchus spp., Scutellonema spp.,Subanguina spp., Trichodorus spp., for example Trichodorus obtusus,Trichodorus primitivus, Tylenchorhynchus spp., for exampleTylenchorhynchus annulatus, Tylenchulus spp., for example Tylenchulussemipenetrans, Xiphinema spp., for example Xiphinema index.

Formulations

The present invention further relates to formulations and use formsprepared therefrom as pesticides, for example drench, drip and sprayliquors, comprising an active compound combination according to theinvention. In some cases, the use forms comprise further pesticidesand/or adjuvants which improve action, such as penetrants, e.g.vegetable oils, for example rapeseed oil, sunflower oil, mineral oils,for example paraffin oils, alkyl esters of vegetable fatty acids, forexample rapeseed oil methyl ester or soya oil methyl ester, or alkanolalkoxylates and/or spreaders, for example alkylsiloxanes and/or salts,for example organic or inorganic ammonium or phosphonium salts, forexample ammonium sulphate or diammonium hydrogenphosphate and/orretention promoters, for example dioctyl sulphosuccinate orhydroxypropyl guar polymers and/or humectants, for example glyceroland/or fertilizers, for example ammonium-, potassium- orphosphorus-containing fertilizers.

Customary formulations are, for example, water-soluble liquids (SL),emulsion concentrates (EC), emulsions in water (EW), suspensionconcentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules(GR) and capsule concentrates (CS); these and further possibleformulation types are described, for example, by Crop Life Internationaland in Pesticide Specifications, Manual on development and use of FAOand WHO specifications for pesticides, FAO Plant Production andProtection Papers—173, prepared by the FAO/WHO Joint Meeting onPesticide Specifications, 2004, ISBN: 9251048576. The formulations, inaddition to the active compound combination according to the invention,optionally comprise further agrochemically active compounds.

These are preferably formulations or use forms which compriseauxiliaries, for example extenders, solvents, spontaneity promoters,carriers, emulsifiers, dispersants, frost protectants, biocides,thickeners and/or further auxiliaries, for example adjuvants. Anadjuvant in this context is a component which enhances the biologicaleffect of the formulation, without the component itself having anybiological effect. Examples of adjuvants are agents which promoteretention, spreading, attachment to the leaf surface or penetration.

These formulations are prepared in a known way, for example by mixingthe active compound combination according to the invention withauxiliaries such as, for example, extenders, solvents and/or solidcarriers and/or other auxiliaries such as, for example, surfactants. Theformulations are prepared either in suitable facilities or else beforeor during application.

The auxiliaries used may be substances suitable for imparting specialproperties, such as certain physical, technical and/or biologicalproperties, to the formulation of the active compound combinationaccording to the invention, or to the use forms prepared from theseformulations (for example ready-to-use pesticides such as spray liquorsor seed dressing products).

Suitable extenders are, for example, water, polar and nonpolar organicchemical liquids, for example from the classes of the aromatic andnon-aromatic hydrocarbons (such as paraffins, alkylbenzenes,alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, ifappropriate, may also be substituted, etherified and/or esterified), theketones (such as acetone, cyclohexanone), the esters (including fats andoils) and (poly)ethers, the unsubstituted and substituted amines,amides, lactams (such as N-alkylpyrrolidones) and lactones, thesulphones and sulphoxides (such as dimethyl sulphoxide), the carbonatesand the nitriles.

If the extender used is water, it is also possible to employ, forexample, organic solvents as auxiliary solvents. Essentially, suitableliquid solvents are: aromatics such as xylene, toluene oralkylnaphthalenes, chlorinated aromatics or chlorinated aliphatichydrocarbons such as chlorobenzenes, chloroethylenes or methylenechloride, aliphatic hydrocarbons such as cyclohexane or paraffins, forexample mineral oil fractions, mineral and vegetable oils, alcohols suchas butanol or glycol and their ethers and esters, ketones such asacetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone,strongly polar solvents such as dimethylformamide or dimethylsulphoxide, carbonates such as propylene carbonate, butylene carbonate,diethyl carbonate or dibutyl carbonate, or nitriles such as acetonitrileor propanenitrile.

In principle, it is possible to use all suitable solvents. Examples ofsuitable solvents are aromatic hydrocarbons, such as xylene, toluene oralkylnaphthalenes, chlorinated aromatic or chlorinated aliphatichydrocarbons, such as chlorobenzene, chloroethylene or methylenechloride, aliphatic hydrocarbons, such as cyclohexane, paraffins,petroleum fractions, mineral and vegetable oils, alcohols, such asmethanol, ethanol, isopropanol, butanol or glycol and their ethers andesters, ketones such as acetone, methyl ethyl ketone, methyl isobutylketone or cyclohexanone, strongly polar solvents, such as dimethylsulphoxide, carbonates such as propylene carbonate, butylene carbonate,diethyl carbonate or dibutyl carbonate, nitriles such as acetonitrile orpropanenitrile, and also water.

In principle, it is possible to use all suitable carriers. Usefulcarriers include especially: for example ammonium salts and groundnatural minerals such as kaolins, clays, talc, chalk, quartz,attapulgite, montmorillonite or diatomaceous earth, and ground syntheticmaterials such as finely divided silica, alumina and natural orsynthetic silicates, resins, waxes and/or solid fertilizers. Mixtures ofsuch carriers can likewise be used. Useful carriers for granulesinclude: for example crushed and fractionated natural rocks such ascalcite, marble, pumice, sepiolite, dolomite, and synthetic granules ofinorganic and organic meals, and also granules of organic material suchas sawdust, paper, coconut shells, corn cobs and tobacco stalks.

Liquefied gaseous extenders or solvents can also be used. Particularlysuitable extenders or carriers are those which are gaseous at ambienttemperature and under atmospheric pressure, for example aerosolpropellant gases, such as halohydrocarbons, and also butane, propane,nitrogen and carbon dioxide.

Examples of emulsifiers and/or foam-formers, dispersants or wettingagents with ionic or nonionic properties, or mixtures of thesesurfactants, are salts of polyacrylic acid, salts of lignosulphonicacid, salts of phenolsulphonic acid or naphthalenesulphonic acid,polycondensates of ethylene oxide with fatty alcohols or with fattyacids or with fatty amines, with substituted phenols (preferablyalkylphenols or arylphenols), salts of sulphosuccinic esters, taurinederivatives (preferably alkyl taurates), isethionate derivatives,phosphoric esters of polyethoxylated alcohols or phenols, fatty estersof polyols, and derivatives of the compounds containing sulphates,sulphonates and phosphates, for example alkylaryl polyglycol ethers,alkylsulphonates, alkyl sulphates, arylsulphonates, proteinhydrolysates, lignosulphite waste liquors and methylcellulose. Thepresence of a surfactant is advantageous if at least one of thecompounds of the active compound combination according to the inventionand/or one of the inert carriers is insoluble in water and when theapplication takes place in water.

It is possible to use colorants such as inorganic pigments, for exampleiron oxide, titanium oxide and Prussian Blue, and organic dyes such asalizarin dyes, azo dyes and metal phthalocyanine dyes, and nutrients andtrace nutrients such as salts of iron, manganese, boron, copper, cobalt,molybdenum and zinc as further auxiliaries in the formulations and theuse forms derived therefrom.

Additional components may be stabilizers, such as low-temperaturestabilizers, preservatives, antioxidants, light stabilizers or otheragents which improve chemical and/or physical stability. Foam formers orantifoams may also be present.

Tackifiers such as carboxymethylcellulose and natural and syntheticpolymers in the form of powders, granules or latices, such as gumarabic, polyvinyl alcohol and polyvinyl acetate, or else naturalphospholipids such as cephalins and lecithins and syntheticphospholipids may also be present as additional auxiliaries in theformulations and the use forms derived therefrom. Further possibleauxiliaries are mineral and vegetable oils.

Optionally, further auxiliaries may be present in the formulations andthe use forms derived therefrom. Examples of such additives includefragrances, protective colloids, binders, adhesives, thickeners,thixotropic agents, penetrants, retention promoters, stabilizers,sequestrants, complexing agents, humectants, spreaders. In general, theactive compound combination according to the invention can be combinedwith any solid or liquid additive commonly used for formulationpurposes.

Useful retention promoters include all those substances which reduce thedynamic surface tension, for example dioctyl sulphosuccinate, orincrease the viscoelasticity, for example hydroxypropylguar polymers.

Suitable penetrants in the present context are all those substanceswhich are usually used for improving the penetration of agrochemicalactive compounds into plants. Penetrants are defined in this context bytheir ability to penetrate from the (generally aqueous) applicationliquor and/or from the spray coating into the cuticle of the plant andthereby increase the mobility of active compounds in the cuticle. Themethod described in the literature (Baur et al., 1997, Pesticide Science51, 131-152) can be used to determine this property. Examples includealcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecylethoxylate (12), fatty acid esters, for example rapeseed oil methylester or soya oil methyl ester, fatty amine alkoxylates, for exampletallowamine ethoxylate (15), or ammonium and/or phosphonium salts, forexample ammonium sulphate or diammonium hydrogenphosphate.

The formulations preferably comprise between 0.00000001 and 98% byweight of the active compound combination according to the invention or,with particular preference, between 0.01% and 95% by weight of theactive compound combination according to the invention, more preferablybetween 0.5% and 90% by weight of the active compound combinationaccording to the invention, based on the weight of the formulation.

The content of the compound of the active compound combination accordingto the invention in the use forms prepared from the formulations (inparticular pesticides) may vary within wide ranges. The concentration ofthe active compound combination according to the invention in the useforms is usually between 0.00000001 and 95% by weight of the activecompound combination according to the invention, preferably between0.00001 and 1% by weight, based on the weight of the use form. Thecompounds are employed in a customary manner appropriate for the useforms.

Plants and Plant Parts

All plants and plant parts can be treated in accordance with theinvention. Here, plants are to be understood to mean all plants andplant parts such as wanted and unwanted wild plants or crop plants(including naturally occurring crop plants), for example cereals (wheat,rice, triticale, barley, rye, oats), maize, soya bean, potato, sugarbeet, sugar cane, tomatoes, pepper, cucumber, melon, carrot, watermelon,onion, lettuce, spinach, leek, beans, Brassica oleracea (e.g. cabbage)and other vegetable species, cotton, tobacco, oilseed rape, and alsofruit plants (with the fruits apples, pears, citrus fruits andgrapevines). Crop plants can be plants which can be obtained byconventional breeding and optimization methods or by biotechnologicaland genetic engineering methods or combinations of these methods,including the transgenic plants and including the plant varieties whichcan or cannot be protected by varietal property rights. Plants should beunderstood to mean all developmental stages, such as seeds, seedlings,young (immature) plants up to mature plants. Plant parts should beunderstood to mean all parts and organs of the plants above and belowground, such as shoot, leaf, flower and root, examples given beingleaves, needles, stalks, stems, flowers, fruit bodies, fruits and seeds,and also tubers, roots and rhizomes. Parts of plants also includeharvested plants or harvested plant parts and vegetative and generativepropagation material, for example seedlings, tubers, rhizomes, cuttingsand seeds.

Treatment according to the invention of the plants and plant parts withthe active compound combination according to the invention is carriedout directly or by allowing the compounds to act on the surroundings,environment or storage space by the customary treatment methods, forexample by immersion, spraying, evaporation, fogging, scattering,painting on, injection and, in the case of propagation material, inparticular in the case of seeds, also by applying one or more coats.

As already mentioned above, it is possible to treat all plants and theirparts according to the invention. In a preferred embodiment, wild plantspecies and plant cultivars, or those obtained by conventionalbiological breeding methods, such as crossing or protoplast fusion, andalso parts thereof, are treated. In a further preferred embodiment,transgenic plants and plant cultivars obtained by genetic engineeringmethods, if appropriate in combination with conventional methods(genetically modified organisms), and parts thereof are treated. Theterm “parts” or “parts of plants” or “plant parts” has been explainedabove. The invention is used with particular preference to treat plantsof the respective commercially customary cultivars or those that are inuse. Plant cultivars are to be understood as meaning plants having newproperties (“traits”) and which have been obtained by conventionalbreeding, by mutagenesis or by recombinant DNA techniques. They can becultivars, varieties, bio- or genotypes.

Transgenic Plant, Seed Treatment and Integration Events

The transgenic plants or plant cultivars (those obtained by geneticengineering) which are to be treated with preference in accordance withthe invention include all plants which, through the geneticmodification, received genetic material which imparts particularadvantageous useful properties (“traits”) to these plants. Examples ofsuch properties are better plant growth, increased tolerance to high orlow temperatures, increased tolerance to drought or to levels of wateror soil salinity, enhanced flowering performance, easier harvesting,accelerated ripening, higher yields, higher quality and/or a highernutritional value of the harvested products, better storage life and/orprocessability of the harvested products. Further and particularlyemphasized examples of such properties are increased resistance of theplants against animal and microbial pests, such as against insects,arachnids, nematodes, mites, slugs and snails owing, for example, totoxins formed in the plants, in particular those formed in the plants bythe genetic material from Bacillus thuringiensis (for example by thegenes CryIA(a), CryIA(b), CryIA(c), CryIIA, CryIIIA, CryIIIB2, Cry9cCry2Ab, Cry3Bb and CryIF and also combinations thereof), furthermoreincreased resistance of the plants against phytopathogenic fungi,bacteria and/or viruses owing, for example, to systemic acquiredresistance (SAR), systemin, phytoalexins, elicitors and also resistancegenes and correspondingly expressed proteins and toxins, and alsoincreased tolerance of the plants to certain herbicidally activecompounds, for example imidazolinones, sulphonylureas, glyphosate orphosphinothricin (for example the “PAT” gene). The genes which impartthe desired traits in question may also be present in combinations withone another in the transgenic plants. Examples of transgenic plantswhich may be mentioned are the important crop plants, such as cereals(wheat, rice, triticale, barley, rye, oats), maize, soya beans,potatoes, sugar beet, sugar cane, tomatoes, peas and other types ofvegetable, cotton, tobacco, oilseed rape and also fruit plants (with thefruits apples, pears, citrus fruits and grapes), with particularemphasis being given to maize, soya beans, wheat, rice, potatoes,cotton, sugar cane, tobacco and oilseed rape. Traits which areparticularly emphasized are the increased resistance of the plants toinsects, arachnids, nematodes and slugs and snails.

Crop Protection Types of Treatment

The treatment of the plants and plant parts with the compounds of theactive compound combination according to the invention is carried outdirectly or by action on their surroundings, habitat or storage spaceusing customary treatment methods, for example by dipping, spraying,atomizing, irrigating, evaporating, dusting, fogging, broadcasting,foaming, painting, spreading-on, injecting, watering (drenching), dripirrigating and, in the case of propagation material, in particular inthe case of seed, furthermore as a powder for dry seed treatment, asolution for liquid seed treatment, a water-soluble powder for slurrytreatment, by incrusting, by coating with one or more coats, etc. It isfurthermore possible to apply the active compound combination accordingto the invention by the ultra-low volume method or to inject theapplication form or the active compound combination according to theinvention itself into the soil.

A preferred direct treatment of the plants is foliar application, i.e.the active compound combination according to the invention is applied tothe foliage, where treatment frequency and the application rate shouldbe adjusted according to the level of infestation with the pest inquestion.

In the case of systemically active compounds, the active compoundcombination according to the invention also access the plants via theroot system. The plants are then treated by the action of the activecompound combination according to the invention on the habitat of theplant. This may be done, for example, by drenching, or by mixing intothe soil or the nutrient solution, i.e. the locus of the plant (e.g.soil or hydroponic systems) is impregnated with a liquid form of theactive compound combination according to the invention, or by soilapplication, i.e. the active compound combination according to theinvention is introduced in solid form (e.g. in the form of granules)into the locus of the plants, or by drip application (often alsoreferred to as “chemigation”), i.e. the liquid application of the activecompound combination according to the invention from surface orsub-surface driplines over a certain period of time together withvarying amounts of water at defined locations in the vicinity of theplants. In the case of paddy rice crops, this can also be done bymetering the active compound combination according to the invention in asolid application form (for example as granules) into a flooded paddyfield.

Treatment of Seed

The control of animal pests by treating the seed of plants has beenknown for a long time and is the subject of continuous improvements.However, the treatment of seed entails a series of problems which cannotalways be solved in a satisfactory manner. Thus, it is desirable todevelop methods for protecting the seed and the germinating plant whichdispense with, or at least reduce considerably, the additionalapplication of pesticides during storage, after sowing or afteremergence of the plants. It is furthermore desirable to optimize theamount of active compound employed in such a way as to provide optimumprotection for the seed and the germinating plant from attack by animalpests, but without damaging the plant itself by the active compoundemployed. In particular, methods for the treatment of seed should alsotake into consideration the intrinsic insecticidal or nematicidalproperties of pest-resistant or -tolerant transgenic plants in order toachieve optimum protection of the seed and also the germinating plantwith a minimum of pesticides being employed.

The present invention therefore in particular also relates to a methodfor the protection of seed and germinating plants, from attack by pests,by treating the seed with an active compound combination according tothe invention. The method according to the invention for protecting seedand germinating plants against attack by pests furthermore comprises amethod where the seed is treated simultaneously in one operation orsequentially with the compound of formula (I) and the mixing partner ofgroup (II). It also comprises a method where the seed is treated atdifferent times with the compound of formula (I) and the mixing partnerof group (II).

The invention likewise relates to the use of the active compoundcombination according to the invention for the treatment of seed forprotecting the seed and the resulting plant from animal pests.

Furthermore, the invention relates to seed which has been treated withan active compound combination according to the invention so as toafford protection from animal pests. The invention also relates to seedwhich has been treated simultaneously with an active compoundcombination according to the invention. The invention furthermorerelates to seed which has been treated at different times with thecompound of formula (I) and the mixing partner of group (II). In thecase of seed which has been treated at different points in time with anactive compound combination according to the invention, the individualsubstances may be present on the seed in different layers. Here, thelayers comprising a compound of the formula (I) and a mixing partner ofgroup (II) may optionally be separated by an intermediate layer. Theinvention also relates to seed where a compound of the formula (I) and amixing partner of group (II) have been applied as component of a coatingor as a further layer or further layers in addition to a coating.

Furthermore, the invention relates to seed which, after the treatmentwith an active compound combination according to the invention, issubjected to a film-coating process to prevent dust abrasion on theseed.

One of the advantages encountered with a systemically acting activecompound combination according to the invention is the fact that, bytreating the seed, not only the seed itself but also the plantsresulting therefrom are, after emergence, protected against animalpests. In this manner, the immediate treatment of the crop at the timeof sowing or shortly thereafter can be dispensed with.

It has to be considered a further advantage that by treatment of theseed with an active compound combination according to the invention,germination and emergence of the treated seed may be enhanced.

It is likewise to be considered advantageous that an active compoundcombination according to the invention can be used in particular alsofor transgenic seed.

Furthermore, active compound combinations according to the invention canbe employed in combination with compositions or compounds of signallingtechnology, leading to better colonization by symbionts such as, forexample, rhizobia, mycorrhizae and/or endophytic bacteria or fungi,and/or to optimized nitrogen fixation.

The active compound combinations according to the invention are suitablefor protection of seed of any plant variety which is used inagriculture, in the greenhouse, in forests or in horticulture. Inparticular, this takes the form of seed of cereals (for example wheat,barley, rye, millet and oats), corn, cotton, soya beans, rice, potatoes,sunflowers, coffee, tobacco, canola, oilseed rape, beets (for examplesugarbeets and fodder beets), peanuts, vegetables (for example tomatoes,cucumbers, bean, cruciferous vegetables, onions and lettuce), fruitplants, lawns and ornamental plants. The treatment of the seed ofcereals (such as wheat, barley, rye and oats), maize, soya beans,cotton, canola, oilseed rape, vegetables and rice is of particularimportance.

As already mentioned above, the treatment of transgenic seed with anactive compound combination according to the invention is also ofparticular importance. This takes the form of seed of plants which, as arule, comprise at least one heterologous gene which governs theexpression of a polypeptide with in particular insecticidal and/ornematicidal properties. The heterologous genes in transgenic seed canoriginate from microorganisms such as Bacillus, Rhizobium, Pseudomonas,Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. The presentinvention is particularly suitable for the treatment of transgenic seedwhich comprises at least one heterologous gene originating from Bacillussp. It is particularly preferably a heterologous gene derived fromBacillus thuringiensis.

In the context of the present invention, the active compound combinationaccording to the invention is applied to the seed. Preferably, the seedis treated in a state in which it is stable enough to avoid damageduring treatment. In general, the seed may be treated at any point intime between harvest and sowing. The seed usually used has beenseparated from the plant and freed from cobs, shells, stalks, coats,hairs or the flesh of the fruits. For example, it is possible to useseed which has been harvested, cleaned and dried down to a moisturecontent which allows storage. Alternatively, it is also possible to useseed which, after drying, has been treated with, for example, water andthen dried again, for example priming. In the case of rice seed, it isalso possible to use seed which has been soaked, for example in water toa certain stage of the rice embryo (‘pigeon breast stage’), stimulatingthe germination and a more uniform emergence.

When treating the seed, care must generally be taken that the amount ofthe active compound combination according to the invention applied tothe seed and/or the amount of further additives is chosen in such a waythat the germination of the seed is not adversely affected, or that theresulting plant is not damaged. This must be ensured particularly in thecase of active compounds which can exhibit phytotoxic effects at certainapplication rates.

In general, the active compound combinations according to the inventionare applied to the seed in a suitable formulation. Suitable formulationsand processes for seed treatment are known to the person skilled in theart.

The active compound combinations according to the invention can beconverted to the customary seed dressing formulations, such assolutions, emulsions, suspensions, powders, foams, slurries or othercoating compositions for seed, and also ULV formulations.

These formulations are prepared in a known manner, by mixing the activecompound combinations according to the invention with customaryadditives such as, for example, customary extenders and also solvents ordiluents, colorants, wetting agents, dispersants, emulsifiers,antifoams, preservatives, secondary thickeners, adhesives, gibberellinsand also water.

Colorants which may be present in the seed-dressing formulations whichcan be used in accordance with the invention are all colorants which arecustomary for such purposes. It is possible to use either pigments,which are sparingly soluble in water, or dyes, which are soluble inwater. Examples include the dyes known by the names Rhodamine B, C.I.Pigment Red 112 and C.I. Solvent Red 1.

Useful wetting agents which may be present in the seed dressingformulations usable in accordance with the invention are all substanceswhich promote wetting and which are conventionally used for theformulation of agrochemically active compounds. Preference is given tousing alkylnaphthalenesulphonates, such as diisopropyl- ordiisobutylnaphthalenesulphonates.

Useful dispersants and/or emulsifiers which may be present in the seeddressing formulations usable in accordance with the invention are allnonionic, anionic and cationic dispersants conventionally used for theformulation of active agrochemical ingredients. Preference is given tousing nonionic or anionic dispersants or mixtures of nonionic or anionicdispersants. Suitable nonionic dispersants include in particularethylene oxide/propylene oxide block polymers, alkylphenol polyglycolethers and tristryrylphenol polyglycol ethers, and the phosphated orsulphated derivatives thereof. Suitable anionic dispersants are inparticular lignosulphonates, polyacrylic acid salts andarylsulphonate/formaldehyde condensates.

Antifoams which may be present in the seed dressing formulations usablein accordance with the invention are all foam-inhibiting substancesconventionally used for the formulation of active agrochemicalingredients. Preference is given to using silicone antifoams andmagnesium stearate.

Preservatives which may be present in the seed dressing formulationsusable in accordance with the invention are all substances usable forsuch purposes in agrochemical compositions. Examples includedichlorophene and benzyl alcohol hemiformal.

Secondary thickeners which may be present in the seed dressingformulations usable in accordance with the invention are all substanceswhich can be used for such purposes in agrochemical compositions.Cellulose derivatives, acrylic acid derivatives, xanthan, modified claysand finely divided silica are preferred.

Adhesives which may be present in the seed dressing formulations usablein accordance with the invention are all customary binders usable inseed dressing products. Polyvinylpyrrolidone, polyvinyl acetate,polyvinyl alcohol and tylose may be mentioned as being preferred.

Gibberellins which can be present in the seed-dressing formulationswhich can be used in accordance with the invention are preferably thegibberellins A1, A3 (=gibberellic acid), A4 and A7; gibberellic acid isespecially preferably used. The gibberellins are known (cf. R. Wegler“Chemie der Pflanzenschutz- and Schädlingsbekämpfungsmittel”, vol. 2,Springer Verlag, 1970, pp. 401-412).

The seed dressing formulations usable in accordance with the inventioncan be used to treat a wide variety of different kinds of seed eitherdirectly or after prior dilution with water. For instance, theconcentrates or the preparations obtainable therefrom by dilution withwater can be used to dress the seed of cereals, such as wheat, barley,rye, oats, and triticale, and also the seed of maize, rice, oilseedrape, peas, beans, cotton, sunflowers, soya beans and beets, or else awide variety of different vegetable seed. The seed dressing formulationsusable in accordance with the invention, or the dilute use formsthereof, can also be used to dress seed of transgenic plants.

For treatment of seed with the seed dressing formulations usable inaccordance with the invention, or the use forms prepared therefrom byadding water, all mixing units usable customarily for the seed dressingare useful. Specifically, the procedure in the seed dressing is to placethe seed into a mixer, operated batch-wise or continuously, to add theparticular desired amount of seed dressing formulations, either as suchor after prior dilution with water, and to mix everything until theformulation is distributed homogeneously on the seed. If appropriate,this is followed by a drying operation.

The application rate of the seed dressing formulations usable inaccordance with the invention can be varied within a relatively widerange. It is guided by the particular content of the active compoundcombinations according to the invention in the formulations and by theseed. The application rates of the active compound combinationsaccording to the invention are generally between 0.001 and 50 g perkilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.

Vector Control

The active compound combinations according to the invention can also beused in vector control. For the purpose of the present invention, avector is an arthropod, in particular an insect or arachnid, capable oftransmitting pathogens such as, for example, viruses, worms, single-cellorganisms and bacteria from a reservoir (plant, animal, human, etc.) toa host. The pathogens can be transmitted either mechanically (forexample trachoma by non-stinging flies) to a host, or by injection (forexample malaria parasites by mosquitoes) into a host.

Examples of vectors and the diseases or pathogens they transmit are:

1) Mosquitoes

Anopheles: malaria, filariasis;

Culex: Japanese encephalitis, other viral diseases, filariasis,transmission of other worms;

Aedes: yellow fever, dengue fever, other viral diseases, filariasis;

Simuliidae: transmission of worms, in particular Onchocerca volvulus;

Psychodidae: transmission of leishmaniasis

2) Lice: skin infections, epidemic typhus;

3) Fleas: plague, endemic typhus, cestodes;

4) Flies: sleeping sickness (trypanosomiasis); cholera, other bacterialdiseases;

5) Mites: acariosis, epidemic typhus, rickettsialpox, tularaemia, SaintLouis encephalitis, tick-borne encephalitis (TBE), Crimean-Congohaemorrhagic fever, borreliosis;

6) Ticks: borellioses such as Borrelia burgdorferi sensu lato., Borreliaduttoni, tick-borne encephalitis, Q fever (Coxiella burnetii),babesioses (Babesia canis canis), ehrlichiosis.

Examples of vectors in the sense of the present invention are insects,for example aphids, flies, leafhoppers or thrips, which are capable oftransmitting plant viruses to plants. Other vectors capable oftransmitting plant viruses are spider mites, lice, beetles andnematodes.

Further examples of vectors in the sense of the present invention areinsects and arachnids such as mosquitoes, in particular of the generaAedes, Anopheles, for example A. gambiae, A. arabiensis, A. funestus, A.dirus (malaria) and Culex, psychodids such as Phlebotomus, Lutzomyia,lice, fleas, flies, mites and ticks capable of transmitting pathogens toanimals and/or humans.

Vector control is also possible if the active compound combinationsaccording to the invention are resistance-breaking.

Active compound combinations according to the invention are suitable foruse in the prevention of diseases and/or pathogens transmitted byvectors. Thus, a further aspect of the present invention is the use ofactive compound combinations according to the invention for vectorcontrol, for example in agriculture, in horticulture, in gardens and inleisure facilities, and also in the protection of materials and storedproducts.

Protection of Industrial Materials

The active compound combinations according to the invention are suitablefor protecting industrial materials against attack or destruction byinsects, for example from the orders Coleoptera, Hymenoptera, Isoptera,Lepidoptera, Psocoptera and Zygentoma.

Industrial materials in the present context are understood to meaninanimate materials, such as preferably plastics, adhesives, sizes,papers and cards, leather, wood, processed wood products and coatingcompositions. The use of the invention for protecting wood isparticularly preferred.

In a further embodiment, the active compound combinations according tothe invention are used together with at least one further insecticideand/or at least one fungicide.

In a further embodiment, the active compound combinations according tothe invention are present as a ready-to-use pesticide, i.e. they can beapplied to the material in question without further modifications.Suitable further insecticides or fungicides are in particular thosementioned above.

Surprisingly, it has also been found that the active compoundcombinations according to the invention can be employed for protectingobjects which come into contact with saltwater or brackish water, inparticular hulls, screens, nets, buildings, moorings and signallingsystems, against fouling. Likewise, the active compound combinationsaccording to the invention, alone or in combinations with other activecompounds, can be used as antifouling agents.

The plants listed can be treated particularly advantageously accordingto the invention with the active compound combinations according to theinvention. The preferred ranges given above in the active compoundcombinations also apply to the treatment of these plants. Particularemphasis is placed on the plant treatment with the active compoundcombinations specifically mentioned in the present text.

The good effect of the active compound combinations according to theinvention is evident from the following examples. While the individualactive substances have weaknesses in effect, the combinations show aneffect which goes beyond a simple effect-summation. A synergistic effectis always present when the action of the active compound combinations isgreater than the sum of the effects of the individually applied activecompounds.

EXAMPLES

Formula for the Efficacy of the Combination of Two Compounds

-   -   The expected efficacy of a given combination of two compounds is        calculated as follows (see Colby, S. R., “Calculating        Synergistic and antagonistic Responses of Herbicide        Combinations”, Weeds 15, pp. 20-22, 1967):        -   If        -   X is the efficacy expressed in % mortality of the untreated            control for test compound A at a concentration of m ppm            respectively m g/ha,        -   Y is the efficacy expressed in % mortality of the untreated            control for test compound B at a concentration of n ppm            respectively n g/ha,        -   E is the efficacy expressed in % mortality of the untreated            control using the mixture of A and B at m and n ppm            respectively m and n g/ha,        -   then is

$E = {X + Y - \frac{X \times Y}{100}}$

-   -   -   If the observed insecticidal efficacy of the combination is            higher than the one calculated as “E”, then the combination            of the two compounds is more than additive, i.e. there is a            synergistic effect.

Example A

Myzus persicae Spray Test

-   -   Solvent: 78.0 parts by weight acetone 1.5 parts by weight        dimethylformamide    -   Emulsifier: alkylarylpolyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvents and isdiluted with water, containing an emulsifier concentration of 1000 ppm,to the desired concentration. To produce a suitable preparation of aspore suspension the spores are diluted with emulsifier containing waterto the desired concentration. Further test concentrations are preparedby dilution with emulsifier containing water.

Chinese cabbage (Brassica pekinensis) leaf disks infected with allinstars of the green peach aphid (Myzus persicae), are sprayed with apreparation of the active ingredient of the desired concentration.

After the specified period of time, mortality in % is determined. 100%means all aphids have been killed; 0% means none of the aphids have beenkilled. The mortality values determined thus are recalculated using theColby-formula (see above).

According to the present application in this test e.g. the followingcombinations showed a synergistic effect in comparison to the singlecompounds:

TABLE A Myzus persicae - spray test Efficacy Concentration in % afterActive Ingredient in g ai/ha 6 days Compound (Cpd) of formula (I) 8 0 20 Cyenopyrafen 2 0 0.5 0 obs.* cal.** Cpd of formula (I) + Cyenopyrafen8 + 2   70 0 (4:1) (4:1) according to the invention 2 + 0.5 70 0Compound (Cpd) of formula (IIa) 16 0 obs.* cal.** Cpd of formula (I) +Cpd of formula 8 + 16  70 0 (IIa) (1:2) according to the invention *obs.= observed insecticidal efficacy, **cal. = efficacy calculated withColby-formula

Example B

Tetranychus urticae—Spray Test OP-Resistant

-   -   Solvent: 78.0 parts by weight acetone 1.5 parts by weight        dimethylformamide    -   Emulsifier: alkylarylpolyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvents and isdiluted with water, containing an emulsifier concentration of 1000 ppm,to the desired concentration. To produce a suitable preparation of aspore suspension the spores are diluted with emulsifier containing waterto the desired concentration. Further test concentrations are preparedby dilution with emulsifier containing water.

French bean (Phaseolus vulgaris) leaf disks infected with all instars ofthe two spotted spidermite (Tetranychus urticae), are sprayed with apreparation of the active ingredient of the desired concentration.

After the specified period of time, mortality in % is determined. 100%means all spider mites have been killed and 0% means none of the spidermites have been killed. The mortality values determined thus arerecalculated using the Colby-formula (see above).

According to the present application in this test e.g. the followingcombinations showed a synergistic effect in comparison to the singlecompounds:

TABLE B-1 Tetranychus urticae - spray test Efficacy Concentration in %after Active Ingredient in g ai/ha 2 days Cpd of formula (I) 0.5 0 0.125 0 Abamectin   0.00125 0 obs.* cal.** Cpd of formula (I) +Abamectin (400:1)   0.5 + 0.00125 70  0 according to the invention (Cpd)of formula (IIa) 1   0 obs.* cal.** Cpd of formula (I) + Cpd of formula(IIa) (1:2) 0.5 + 1   70  0 according to the invention (Cpd) of formula(IIb) 0.5 0 obs.* cal.** Cpd of formula (I) + Cpd of formula (IIb) (1:1)0.5 + 0.5  70  0 according to the invention Cyflumetofen 0.5 0 obs.*cal.** Cpd of formula (I) + Cyflumetofen (1:1) 0.5 + 0.5  90  0according to the invention Emamectin-benzoate   0.0125 0    0.003125 0obs.* cal.** Cpd of formula (I) + Emamectin-benzoate (40:1)  0.5 +0.0125 70  0 (40:1) according to the invention  0.125 + 0.003125 70  0Pyflubumide   0.0125 0 obs.* cal.** Cpd of formula (I) + Pyflubumide(10:1) 0.125 + 0.0125 70  0 according to the invention  0.125 0 Spinosad  0.03125 0 obs.* cal.** Cpd of formula (I) + Spinosad (4:1)  0.5 +0.125 90  0 according to the invention  0.125 + 0.03125 70  0Spiromesifen  0.05 0 obs.* cal.** Cpd of formula (I) + Spiromesifen(10:1) 0.5 + 0.05 90  0 according to the invention Spirotetramat  0.05 0obs.* cal.** Cpd of formula (I) + Spirotetramat (10:1) 0.5 + 0.05 70  0according to the invention

TABLE B-2 Tetranychus urticae - spray test Efficacy Concentration in %after Active Ingredient in g ai/ha 6 days Cpd of formula (I) 0.6  0 0.5 0 0.3  0  0.125  0 Abamectin  0.03 70  0.015 70 obs.* obs.* cal.** Cpdof formula (I) + Abamectin (20:1) 0.6 + 0.03 100   70 (20:1)  0.3 +0.015 100   70 according to the invention Cpd of formula (IIa) 1   0obs.* cal.** Cpd of formula (I) + Cpd of formula (IIa) (1:2) 0.5 + 1  90 0 according to the invention Cpd of formula (IIb) 0.5 0 obs.* cal.**Cpd of formula (I) + Cpd of formula (IIb) (1:1) 0.5 + 0.5  70 0according to the invention Cyenopyrafen  0.125 0 obs.* cal.** Cpd offormula (I) + Cyenopyrafen (4:1)  0.5 + 0.125 70 0 according to theinvention Cyflumetofen 0.5 0 obs.* cal.** Cpd of formula (I) +Cyflumetofen (1:1) 0.5 + 0.5  90 0 according to the inventionEmamectin-benzoate  0.15 0   0.0125 0    0.003125 0 obs.* cal.** Cpd offormula (I) + Emamectin-benzoate (4:1) 0.6 + 0.15 90 0 (40:1)  0.5 +0.0125 70 0 (40:1) according to the invention  0.125 + 0.003125 70 0Milbemectin 1.5 0  0.75 0 obs.* cal.** Cpd of formula (I) + Milbemectin(1:2.5) 0.6 + 1.5  90 0 (1:2.5) according to the invention 0.3 + 0.75 700 Pyflubumide 0.6 70    0.0125 0 obs.* cal.** Cpd of formula (I) +Pyflubumide (1:1) 0.6 + 0.6  100  70  (10:1) according to the invention0.125 + 0.0125 90 0 Spinosad  0.125 0   0.03125 0  0.5 + 0.125 obs.*cal.** Cpd of formula (I) + Spinosad (4:1)  0.125 + 0.03125 90 0according to the invention 70 0 Spiromesifen 0.6 0  0.05 0 obs.* cal.**Cpd of formula (I) + Spiromesifen (1:1) 0.6 + 0.6  70 0 (10:1) accordingto the invention 0.5 + 0.05 90 0 Spirotetramat  0.05 0 obs.* cal.** Cpdof formula (I) + Spirotetramat 0.5 + 0.05 90 0 (10:1) according to theinvention *obs. = observed insecticidal efficacy, **cal. = efficacycalculated with Colby-formula

Example C

Tetranychus urticae Spray Test; OP-Resistant

Solvent: 7 parts by weight of dimethylformamide

Emulsifier: alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent and isdiluted with water, containing an emulsifier concentration of 1000 ppm,to the desired concentration. Further test concentrations are preparedby dilution with emulsifier containing water.

Bean plants (Phaseolus vulgaris) which are heavily infested with allstages of the two-spotted spider mite (Tetranychus urticae) are treatedby being sprayed with the preparation of the active compound of thedesired concentration.

After the specified period of time mortality in % is determined. 100%means all the spider mites have been killed and 0% means none of thespider mites have been killed. The mortality values determined thus arerecalculated using the Colby-formula (see above).

According to the present application in this test e.g. the followingcombinations showed a synergistic effect in comparison to the singlecompounds:

TABLE C-1 Tetranychus urticae - spray test Efficacy Concentration in %after Active Ingredient in ppm 3 days Cpd of formula (I) 0.4 0 Abamectin0.01 0 obs.* cal.** Cpd of formula (I) + Abamectin 0.4 + 0.01 40  0(40:1) according to the invention

TABLE C-2 Tetranychus urticae - spray test Efficacy Concentration in %after Active Ingredient in ppm 7 days Cpd of formula (I) 0.8 30Spirotetramat 2 40 obs.* cal.** Cpd of formula (I) + Spirotetramat 0.8 +2 90 58 (1:2.5) according to the invention *obs. = observed insecticidalefficacy, **cal. = efficacy calculated with Colby-formula

Example D

Meloidogyne incognita—Test

Solvent: 125.0 parts by weight of acetone

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent, and theconcentrate is diluted with water to the desired concentration. Toproduce a suitable preparation of a spore suspension the spores arediluted with water to the desired concentration.

Vessels are filled with sand, a solution of the active ingredient, asuspension containing eggs and larvae of the southern root-knot nematode(Meloidogyne incognita) and salad seeds. The salad seeds germinate andthe seedlings grow. Galls develop in the roots.

After the specified period of time nematicidal activity is determined onthe basis of the percentage of gall formation. 100% means no galls werefound and 0% means the number of galls found on the roots of the treatedplants was equal to that in untreated control plants.

According to the present application in this test e.g. the followingcombinations showed a synergistic effect in comparison to the singlecompounds:

TABLE D Meloidogyne incognita - test Efficacy Concentration in % afterActive Ingredient in ppm 14 days Cpd of formula (I) 2 70  1 0Spirotetramat 60 0 30 0 obs.* cal.** Cpd of formula (I) + Spirotetramat2 + 60 100  70 (1:30) according to the invention 1 + 30 70  0 *obs. =observed insecticidal efficacy, **cal. = efficacy calculated withColby-formula

The invention claimed is:
 1. An active compound combination comprisingat least one compound of formula (I)

and at least one active compound of group (II) which is selected fromthe group consisting of (II-1) abamectin, (II-2) emamectin benzoate,(II-4) milbemectin, (II-6) spiromesifen, (II-7) spirotetramat, (II-8)cyenopyrafen, (II-9) cyflumetofen, (II-10) spinosad and (II-14)pyflubumide, or is selected from the group consisting of a compound offormula (IIa)

and a compound of formula (IIb)

wherein the compound combination is synergistically active; and whereinthe mixing ratio of active compound of the formula (I) to (II-10)spinosad is 10:1 to 1:10 based on weight ratio; the mixing ratios ofactive compound of the formula (I) to (II-1) abamectin, to (II-2)emamectin benzoate and to (II-4) milbemectin are 400:1 to 1:1, 50:1 to1:1 and 5:1 to 1:5, respectively, each based on weight ratio; the mixingratios of active compound of the formula (I) to (II-6) spiromesifen andto (II-7) spirotetramat are 20:1 to 1:10 and 30:1 to 1:30, respectively,each based on weight ratio; the mixing ratios of active compound of theformula (I) to (II-8) cyenopyrafen, to (II-9) cyflumetofen and to(II-14) pyflubumide are 10:1 to 1:10, 10:1 to 1:5 and 20:1 to 1:10,respectively, each based on weight ratio; and the mixing ratio of activecompound of the formula (I) to compounds of formula (IIa) or (IIb) is10:1 to 1:10, based on weight ratio.
 2. The active compound combinationaccording to claim 1, wherein the compound of formula (I) is present inform of a (+) enantiomer, or is present in form of a mixture of (+)enantiomer and (−) enantiomer which is enriched in the (+) enantiomer.3. The active compound combination according to claim 2, wherein thecompound of formula (I) is present in the form of a mixture of (+)enantiomer and (−) enantiomer which is enriched in the (+) enantiomer ina mixing ratio of at least 60:40 (+):(−) enantiomer.
 4. A productcomprising the active compound combination as defined in claim 1 forcontrolling one or more animal pests.
 5. The product according to claim4, wherein the animal pest is an insect, arachnid or acarid pest.
 6. Aproduct comprising the active compound combination as defined in claim 1for controlling one or more microbial pests.
 7. A product comprising theactive compound combination as defined in claim 1 for controllingnematodes.
 8. A product comprising the active compound combination asdefined in claim 1 as a plant-strengthening agent.
 9. A productcomprising an active compound combination as defined in claim 1 for seedtreatment.
 10. A product comprising the active compound combination asdefined in claim 1 on one or more transgenic plants.
 11. A productcomprising the active compound combination according to claim 1 fortreating one or more plants or parts thereof selected from the groupconsisting of citrus, pome fruits, stone fruits, tropical fruits, nuts,berries, vegetables, cotton, soybean, grape, tea, coffee, maize, riceand ornamentals.
 12. A method for controlling animal or microbial pests,comprising allowing the active compound combination as defined in claim1 to act on animal or microbial pests and/or a habitat thereof.
 13. Themethod according to claim 12, wherein the animal pest is an insect orarachnid or acarid pest.
 14. A process for preparing a crop protectionagent, comprising mixing the active compound combination as defined inclaim 1 with one or more extenders and/or surfactants.